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Publisher: Medknow Publishers   (Total: 429 journals)

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Showing 1 - 200 of 429 Journals sorted alphabetically
Acta Medica Intl.     Open Access   (SJR: 0.101, CiteScore: 0)
Advanced Arab Academy of Audio-Vestibulogy J.     Open Access  
Advanced Biomedical Research     Open Access  
Advances in Human Biology     Open Access   (Followers: 3)
Advances in Skeletal Muscle Function Assessment     Open Access  
African J. for Infertility and Assisted Conception     Open Access  
African J. of Medical and Health Sciences     Open Access   (Followers: 2)
African J. of Paediatric Surgery     Open Access   (Followers: 7, SJR: 0.25, CiteScore: 1)
African J. of Trauma     Open Access   (Followers: 1)
Ain-Shams J. of Anaesthesiology     Open Access   (Followers: 3)
Al-Azhar Assiut Medical J.     Open Access  
Al-Basar Intl. J. of Ophthalmology     Open Access   (Followers: 1)
Alexandria J. of Pediatrics     Open Access  
Ancient Science of Life     Open Access   (Followers: 5)
Anesthesia : Essays and Researches     Open Access   (Followers: 10)
Annals of African Medicine     Open Access   (Followers: 1, SJR: 0.258, CiteScore: 1)
Annals of Bioanthropology     Open Access   (Followers: 4)
Annals of Cardiac Anaesthesia     Open Access   (Followers: 14, SJR: 0.308, CiteScore: 1)
Annals of Indian Academy of Neurology     Open Access   (Followers: 3, SJR: 0.434, CiteScore: 1)
Annals of Indian Academy of Otorhinolaryngology Head and Neck Surgery     Open Access  
Annals of Indian Psychiatry     Open Access  
Annals of Maxillofacial Surgery     Open Access   (Followers: 6)
Annals of Medical and Health Sciences Research     Open Access   (Followers: 7)
Annals of Nigerian Medicine     Open Access   (Followers: 1)
Annals of Pediatric Cardiology     Open Access   (Followers: 7, SJR: 0.352, CiteScore: 1)
Annals of Saudi Medicine     Open Access   (SJR: 0.238, CiteScore: 1)
Annals of Thoracic Medicine     Open Access   (Followers: 5, SJR: 0.524, CiteScore: 1)
Annals of Tropical Medicine and Public Health     Open Access   (Followers: 12, SJR: 0.152, CiteScore: 0)
Annals of Tropical Pathology     Open Access  
Apollo Medicine     Open Access  
APOS Trends in Orthodontics     Open Access  
Arab J. of Interventional Radiology     Open Access  
Archives of Cardiovascular Imaging     Open Access   (Followers: 1, SJR: 0.187, CiteScore: 0)
Archives of Intl. Surgery     Open Access   (Followers: 10, SJR: 0.302, CiteScore: 1)
Archives of Medicine and Health Sciences     Open Access   (Followers: 3)
Archives of Medicine and Surgery     Open Access  
Archives of Pharmacy Practice     Open Access   (Followers: 6, SJR: 0.102, CiteScore: 0)
Archives of Trauma Research     Open Access   (Followers: 3, SJR: 0.37, CiteScore: 2)
Asia Pacific J. of Clinical Trials : Nervous System Diseases     Open Access  
Asia-Pacific J. of Oncology Nursing     Open Access   (Followers: 4)
Asian J. of Andrology     Open Access   (Followers: 1, SJR: 0.856, CiteScore: 2)
Asian J. of Neurosurgery     Open Access   (Followers: 2)
Asian J. of Oncology     Open Access   (Followers: 1)
Asian J. of Transfusion Science     Open Access   (Followers: 1, SJR: 0.35, CiteScore: 1)
Asian Pacific J. of Reproduction     Open Access   (SJR: 0.227, CiteScore: 1)
Asian Pacific J. of Tropical Biomedicine     Open Access   (Followers: 2, SJR: 0.491, CiteScore: 2)
Asian Pacific J. of Tropical Medicine     Open Access   (Followers: 1, SJR: 0.561, CiteScore: 2)
Astrocyte     Open Access  
Avicenna J. of Medicine     Open Access   (Followers: 1)
AYU : An international quarterly journal of research in Ayurveda     Open Access   (Followers: 6)
Benha Medical J.     Open Access  
Biomedical and Biotechnology Research J.     Open Access  
BLDE University J. of Health Sciences     Open Access  
Brain Circulation     Open Access  
Bulletin of Faculty of Physical Therapy     Open Access   (Followers: 1)
Canadian J. of Rural Medicine     Full-text available via subscription   (SJR: 0.202, CiteScore: 0)
Cancer Translational Medicine     Open Access   (Followers: 2)
Cardiology Plus     Open Access  
Chinese Medical J.     Open Access   (Followers: 10, SJR: 0.52, CiteScore: 1)
CHRISMED J. of Health and Research     Open Access  
Clinical Cancer Investigation J.     Open Access  
Clinical Dermatology Review     Open Access   (Followers: 2)
Clinical Trials in Degenerative Diseases     Open Access  
Clinical Trials in Orthopedic Disorders     Open Access  
Community Acquired Infection     Open Access  
Conservation and Society     Open Access   (Followers: 10, SJR: 0.811, CiteScore: 2)
Contemporary Clinical Dentistry     Open Access   (Followers: 4, SJR: 0.353, CiteScore: 1)
Current Medical Issues     Open Access   (Followers: 1)
CytoJ.     Open Access   (Followers: 2, SJR: 0.543, CiteScore: 1)
Delta J. of Ophthalmology     Open Access  
Dental Hypotheses     Open Access   (Followers: 3, SJR: 0.152, CiteScore: 0)
Dental Research J.     Open Access   (Followers: 11, SJR: 0.416, CiteScore: 1)
Dentistry and Medical Research     Open Access  
Digital Medicine     Open Access  
Drug Development and Therapeutics     Open Access  
Education for Health     Open Access   (Followers: 6, SJR: 0.242, CiteScore: 0)
Egyptian J. of Bronchology     Open Access  
Egyptian J. of Cardiothoracic Anesthesia     Open Access  
Egyptian J. of Cataract and Refractive Surgery     Open Access   (Followers: 1, SJR: 1.799, CiteScore: 2)
Egyptian J. of Chest Diseases and Tuberculosis     Open Access   (Followers: 3, SJR: 0.155, CiteScore: 0)
Egyptian J. of Dermatology and Venerology     Open Access   (Followers: 1)
Egyptian J. of Haematology     Open Access   (Followers: 1)
Egyptian J. of Internal Medicine     Open Access   (Followers: 1)
Egyptian J. of Neurology, Psychiatry and Neurosurgery     Open Access   (Followers: 1, SJR: 0.127, CiteScore: 0)
Egyptian J. of Obesity, Diabetes and Endocrinology     Open Access  
Egyptian J. of Otolaryngology     Open Access   (Followers: 2)
Egyptian J. of Psychiatry     Open Access   (Followers: 2)
Egyptian J. of Surgery     Open Access   (Followers: 1)
Egyptian Nursing J.     Open Access  
Egyptian Orthopaedic J.     Open Access   (Followers: 2)
Egyptian Pharmaceutical J.     Open Access  
Egyptian Retina J.     Open Access  
Egyptian Rheumatology and Rehabilitation     Open Access  
Endodontology     Open Access  
Endoscopic Ultrasound     Open Access   (SJR: 0.822, CiteScore: 2)
Environmental Disease     Open Access   (Followers: 2)
Eurasian J. of Pulmonology     Open Access  
European J. of Dentistry     Open Access   (Followers: 2, SJR: 0.749, CiteScore: 2)
European J. of General Dentistry     Open Access   (Followers: 1, SJR: 0.12, CiteScore: 0)
European J. of Prosthodontics     Open Access   (Followers: 3)
European J. of Psychology and Educational Studies     Open Access   (Followers: 11, SJR: 0.113, CiteScore: 0)
Fertility Science and Research     Open Access  
Formosan J. of Surgery     Open Access   (SJR: 0.112, CiteScore: 0)
Genome Integrity     Open Access   (Followers: 3, SJR: 0.153, CiteScore: 0)
Glioma     Open Access  
Global J. of Transfusion Medicine     Open Access   (Followers: 1)
Gynecology and Minimally Invasive Therapy     Open Access   (SJR: 0.311, CiteScore: 1)
Hamdan Medical J.     Open Access  
Heart and Mind     Open Access  
Heart India     Open Access   (Followers: 1)
Heart Views     Open Access   (Followers: 2)
Hepatitis B Annual     Open Access   (Followers: 3)
Ibnosina J. of Medicine and Biomedical Sciences     Open Access  
IJS Short Reports     Open Access  
Imam J. of Applied Sciences     Open Access  
Indian Anaesthetists Forum     Open Access  
Indian Dermatology Online J.     Open Access   (Followers: 3)
Indian J. of Allergy, Asthma and Immunology     Open Access   (Followers: 1)
Indian J. of Anaesthesia     Open Access   (Followers: 7, SJR: 0.478, CiteScore: 1)
Indian J. of Burns     Open Access   (Followers: 1)
Indian J. of Cancer     Open Access   (Followers: 1, SJR: 0.361, CiteScore: 1)
Indian J. of Cerebral Palsy     Open Access   (Followers: 1)
Indian J. of Community Medicine     Open Access   (Followers: 2, SJR: 0.37, CiteScore: 1)
Indian J. of Critical Care Medicine     Open Access   (Followers: 2, SJR: 0.604, CiteScore: 1)
Indian J. of Dental Research     Open Access   (Followers: 4, SJR: 0.266, CiteScore: 1)
Indian J. of Dental Sciences     Open Access  
Indian J. of Dentistry     Open Access   (Followers: 1)
Indian J. of Dermatology     Open Access   (Followers: 2, SJR: 0.468, CiteScore: 1)
Indian J. of Dermatology, Venereology and Leprology     Open Access   (Followers: 5, SJR: 0.445, CiteScore: 1)
Indian J. of Dermatopathology and Diagnostic Dermatology     Open Access  
Indian J. of Drugs in Dermatology     Open Access   (Followers: 1, SJR: 0.791, CiteScore: 1)
Indian J. of Endocrinology and Metabolism     Open Access   (Followers: 4, SJR: 0.568, CiteScore: 1)
Indian J. of Health Sciences     Open Access   (Followers: 3)
Indian J. of Medical and Paediatric Oncology     Open Access   (SJR: 0.425, CiteScore: 1)
Indian J. of Medical Microbiology     Open Access   (Followers: 1, SJR: 0.503, CiteScore: 1)
Indian J. of Medical Research     Open Access   (Followers: 4, SJR: 0.656, CiteScore: 1)
Indian J. of Medical Sciences     Open Access   (Followers: 2, SJR: 0.102, CiteScore: 0)
Indian J. of Multidisciplinary Dentistry     Open Access   (Followers: 1)
Indian J. of Nephrology     Open Access   (Followers: 2, SJR: 0.347, CiteScore: 1)
Indian J. of Nuclear Medicine     Open Access   (Followers: 2, SJR: 0.23, CiteScore: 0)
Indian J. of Occupational and Environmental Medicine     Open Access   (Followers: 3, SJR: 0.225, CiteScore: 1)
Indian J. of Ophthalmology     Open Access   (Followers: 4, SJR: 0.498, CiteScore: 1)
Indian J. of Oral Health and Research     Open Access  
Indian J. of Oral Sciences     Open Access   (Followers: 1)
Indian J. of Orthopaedics     Open Access   (Followers: 8, SJR: 0.392, CiteScore: 1)
Indian J. of Otology     Open Access   (Followers: 1, SJR: 0.199, CiteScore: 0)
Indian J. of Paediatric Dermatology     Open Access   (Followers: 2)
Indian J. of Pain     Open Access   (Followers: 1)
Indian J. of Palliative Care     Open Access   (Followers: 5, SJR: 0.454, CiteScore: 1)
Indian J. of Pathology and Microbiology     Open Access   (Followers: 2, SJR: 0.276, CiteScore: 1)
Indian J. of Pharmacology     Open Access   (SJR: 0.412, CiteScore: 1)
Indian J. of Plastic Surgery     Open Access   (Followers: 12, SJR: 0.311, CiteScore: 0)
Indian J. of Psychiatry     Open Access   (Followers: 3, SJR: 0.408, CiteScore: 1)
Indian J. of Psychological Medicine     Open Access   (SJR: 0.368, CiteScore: 1)
Indian J. of Public Health     Open Access   (Followers: 1)
Indian J. of Radiology and Imaging     Open Access   (Followers: 4)
Indian J. of Research in Homoeopathy     Open Access  
Indian J. of Respiratory Care     Open Access  
Indian J. of Rheumatology     Open Access   (SJR: 0.119, CiteScore: 0)
Indian J. of Sexually Transmitted Diseases and AIDS     Open Access   (Followers: 2, SJR: 0.34, CiteScore: 0)
Indian J. of Social Psychiatry     Open Access   (Followers: 2)
Indian J. of Transplantation     Open Access  
Indian J. of Urology     Open Access   (Followers: 3, SJR: 0.434, CiteScore: 1)
Indian J. of Vascular and Endovascular Surgery     Open Access   (Followers: 2)
Indian Spine J.     Open Access  
Industrial Psychiatry J.     Open Access   (Followers: 2)
Intervention     Open Access   (Followers: 1)
Intl. Archives of Health Sciences     Open Access  
Intl. J. of Abdominal Wall and Hernia Surgery     Open Access  
Intl. J. of Academic Medicine     Open Access  
Intl. J. of Advanced Medical and Health Research     Open Access  
Intl. J. of Applied and Basic Medical Research     Open Access  
Intl. J. of Clinical and Experimental Physiology     Open Access   (Followers: 1)
Intl. J. of Clinicopathological Correlation     Open Access  
Intl. J. of Community Dentistry     Open Access  
Intl. J. of Critical Illness and Injury Science     Open Access   (Followers: 1, SJR: 0.192, CiteScore: 0)
Intl. J. of Educational and Psychological Researches     Open Access   (Followers: 4)
Intl. J. of Environmental Health Engineering     Open Access   (Followers: 1)
Intl. J. of Forensic Odontology     Open Access   (Followers: 1)
Intl. J. of Green Pharmacy     Open Access   (Followers: 3, SJR: 0.142, CiteScore: 0)
Intl. J. of Growth Factors and Stem Cells in Dentistry     Open Access  
Intl. J. of Health & Allied Sciences     Open Access   (Followers: 3)
Intl. J. of Health System and Disaster Management     Open Access   (Followers: 3)
Intl. J. of Heart Rhythm     Open Access  
Intl. J. of Medicine and Public Health     Open Access   (Followers: 6)
Intl. J. of Mycobacteriology     Open Access   (SJR: 0.535, CiteScore: 1)
Intl. J. of Noncommunicable Diseases     Open Access  
Intl. J. of Nutrition, Pharmacology, Neurological Diseases     Open Access   (Followers: 4, SJR: 0.17, CiteScore: 0)
Intl. J. of Oral Health Sciences     Open Access   (Followers: 2)
Intl. J. of Orofacial Biology     Open Access  
Intl. J. of Orofacial Research     Open Access  
Intl. J. of Orthodontic Rehabilitation     Open Access  
Intl. J. of Pedodontic Rehabilitation     Open Access  
Intl. J. of Pharmaceutical Investigation     Open Access   (Followers: 1)
Intl. J. of Preventive Medicine     Open Access   (Followers: 1, SJR: 0.623, CiteScore: 1)
Intl. J. of Shoulder Surgery     Open Access   (Followers: 5, SJR: 0.653, CiteScore: 1)
Intl. J. of the Cardiovascular Academy     Open Access   (SJR: 0.105, CiteScore: 0)
Intl. J. of Trichology     Open Access   (SJR: 0.4, CiteScore: 1)
Intl. J. of Yoga     Open Access   (Followers: 13)
Intl. J. of Yoga : Philosophy, Psychology and Parapsychology     Open Access   (Followers: 5)

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Journal Cover
Indian Journal of Paediatric Dermatology
Number of Followers: 2  

  This is an Open Access Journal Open Access journal
ISSN (Print) 2319-7250 - ISSN (Online) 2319-7269
Published by Medknow Publishers Homepage  [429 journals]
  • Skin lesions simulating child abuse

    • Authors: Sahana M Srinivas, Celia Moss
      Pages: 187 - 193
      Abstract: Sahana M Srinivas, Celia Moss
      Indian Journal of Paediatric Dermatology 2018 19(3):187-193
      Child abuse is a broad term which describes various forms of maltreatment and neglect in children and is recognized increasingly. Physical abuse presents to dermatologists as well as pediatricians because the skin is so readily accessible for harm. Doctors unfamiliar with the wide range of skin disorders that simulate child abuse may mistakenly diagnose child abuse or “fabricated or induced illness by carers” (Munchausen by proxy), with traumatic consequences for the family. Mimics of child abuse include various cultural practices, birthmarks, bleeding disorders, bacterial infections, bullous diseases, and hereditary conditions. Dermatitis artefacta and self-harm must also be considered. Observation of the skin lesions and their evolution during hospitalization may provide the correct answer, but knowledge of the morphology and presentation of various skin disorders is crucial to avoid incorrect diagnosis of child abuse. This article describes some of the less well-known mimics of child abuse. It is essential that dermatologists support pediatricians in managing conditions that appear unusual and possibly artifactual.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):187-193
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_56_18
      Issue No: Vol. 19, No. 3 (2018)
       
  • Monogenic autoinflammatory syndromes in children: Through the
           dermatologist's lens

    • Authors: Vishal Gupta, M Ramam
      Pages: 194 - 201
      Abstract: Vishal Gupta, M Ramam
      Indian Journal of Paediatric Dermatology 2018 19(3):194-201
      Autoinflammatory syndromes are a group of rare disorders of innate immunity characterized by repeated episodes of inflammation without an obvious cause. Many of these disorders have a childhood onset, and present as recurrent fevers, skin lesions, joint pains and other systemic features. Newer autoinflammatory syndromes with previously undescribed clinical phenotypes are being increasingly recognized. Several of these have distinctive cutaneous manifestations, and dermatologists have an important role to play in the diagnosis of these conditions. Recently, molecular basis for many of these diseases has been identified, thus paving the way for novel targeted therapies. Interleukin-1 blockers have been found to be more effective than the conventional immunosuppressants in their treatment. In this article, we focus on the cutaneous features of well-recognized as well as some of the recently described monogenic autoinflammatory syndromes in children.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):194-201
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_9_18
      Issue No: Vol. 19, No. 3 (2018)
       
  • Pediatric cutaneous tuberculosis: Indian scenario

    • Authors: Bhushan Kumar, Sheetanshu Kumar
      Pages: 202 - 211
      Abstract: Bhushan Kumar, Sheetanshu Kumar
      Indian Journal of Paediatric Dermatology 2018 19(3):202-211
      Burden of tuberculosis still persists in developing countries despite major advances in its treatment strategies. Cutaneous tuberculosis which is a form of extra-pulmonary tuberculosis is seen in a small but significant subset of patients visiting dermatology outpatient services. Cutaneous tuberculosis is characterized by a spectrum of multiple distinct clinical and histopathology presentations. A significant proportion of patients with cutaneous tuberculosis are seen in paediatric age group. Clinical features in children remain mostly the same as that in adults with cutaneous tuberculosis. However, systemic and lymph node involvement and incidence of disseminated disease is observed more commonly in paediatric age group . Awareness among clinicians of the clinical manifestations of cutaneous tuberculosis is of paramount importance for early diagnosis and management of cases with paediatric cutaneous tuberculosis. This would significantly prevent morbidity and complications of the disease . This review aims to discuss the epidemiology, clinical and histopathological features, diagnosis, differential diagnosis and treatment options in children with tuberculosis, especially in the Indian context.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):202-211
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_63_18
      Issue No: Vol. 19, No. 3 (2018)
       
  • Childhood vitiligo: A clinicoepidemiological study

    • Authors: Mrinal Gupta
      Pages: 212 - 214
      Abstract: Mrinal Gupta
      Indian Journal of Paediatric Dermatology 2018 19(3):212-214
      Background: Vitiligo is a chronic disorder of pigmentation which has serious psychosocial implications. Early onset or childhood vitiligo, although clinically similar to adult-onset vitiligo, has been found to have a distinct epidemiological, clinical, therapeutic, and prognostic profile. Aims and Objectives: This study was carried out to study the clinicoepidemiological characteristics of vitiligo in patients aged <18 years. Materials and Methods: It was a prospective, observational study carried out over a period of 1 year in which fifty children having vitiligo were examined. After taking an informed consent from the attendants/parents of the patients, a complete history including age, sex, duration of the disease, family history, history of Koebner's phenomenon, and history of associated diseases was noted. Results: The study group comprised of 29 females and 21 males (male:female 1:1.38), aged between 6 months and 17 years with a mean age of 8.45 ± 2.34 years and the mean age of onset was 5.6 years. The most common clinical subtypes observed in childhood vitiligo were vitiligo vulgaris in 42% (n = 21) followed by focal in 24% (n = 12), segmental in 12% (n = 6), and acrofacial in 10% patients (n = 5). A family history of vitiligo was seen in 16% patients (n = 8). Leukotrichia was observed in four patients, Koebner phenomenon in 5, and halo nevus in one patient. Conclusions: Childhood vitiligo is a common entity with vitiligo vulgaris being the most common subtype and lower limbs being the most common site of involvement. Children with positive family history had an earlier age of onset, and thyroid abnormalities were more common in nonsegmental variant.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):212-214
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_91_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Cutaneous markers of spinal dysraphism: A cross sectional study

    • Authors: Farhana Tahseen Taj
      Pages: 215 - 219
      Abstract: Farhana Tahseen Taj
      Indian Journal of Paediatric Dermatology 2018 19(3):215-219
      Background: Spinal dysraphism is a rare condition where there are many cutaneous markers which will help a dermatologist to arrive at early diagnosis and prevent complications. Aims and Objectives: The aim and objectives of this are to study the various cutaneous marker of spinal dysraphism in neonatal period and its importance of recognizing early to plan for further management. Materials and Methods: Neonates were examined for cutaneous signs of spinal dysraphism in the first 4 weeks of life. Both occult and open spinal dysraphism clinical features were recorded. Detail history was recorded with respect to age of the mother, parity, consanguinity, and folic acid supplementation. Diagnosis was made clinically. Biopsy is not done as it may introduce infection into spinal canal. Results: A total of 1000 neonates were examined, out of which cutaneous signs of spinal dysraphism were seen in 135 (13.5%) newborns. Sacral dimple was most common seen in 128 (12.8%) neonates, meningomyelocele in 5 (0.5%), dermoid cyst in 1 (0.1%) and acrochordons in 1 (0.1%) neonate. Conclusion: Dermatologist should be aware of the cutaneous marker of spinal dysraphism. Although dermatologist has a less role in the management of spinal dysraphism, their early diagnosis will help in the further management and prevent orthopedic, vertebral, and urological complications.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):215-219
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_90_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • A retrospective study of the pattern of sexually transmitted diseases in
           teenagers attending sexually transmitted disease clinic during a 7-year
           period at a tertiary care centre

    • Authors: Jigna P Barot, Avanita D Solanki, Neela M Patel, Khushboo R Modi, Miral B Bodar
      Pages: 220 - 223
      Abstract: Jigna P Barot, Avanita D Solanki, Neela M Patel, Khushboo R Modi, Miral B Bodar
      Indian Journal of Paediatric Dermatology 2018 19(3):220-223
      Background: Adolescent period corresponds to the age group of 10-15 years. While teenage period, which corresponds to 13-19 year of age group, is the stage of psychosocial development. More and more young people are becoming sexually active in their mid-teens making them vulnerable to contracting the STDs. Adolescents especially in urban areas have favorable attitudes toward premarital and extramarital sex. Material and Methods: This is a retrospective study conducted at tertiary care center. Data regarding STD in teenagers (13-19 year) and their sexual behavior from January 2009 to December 2015 was collected from STI clinic. Result: Total number of adolescent attended STI clinic was 381,out of which 200 were male and 181 were female. Most common STD in female was VVC and in male was nodular scabies. out of 381 patients 155 male and 93 female had confessed about indulging in sexual activity.10 patients were tested positive for HIV and 11 patients were tested positive for syphilis. Conclusion: There is increasing incidence & prevalence of STDs in adolescents due to risky sexual behavior. It is essential to include sex education in teaching methods.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):220-223
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_100_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Efficacy and safety of propranolol on the proliferative phase of infantile
           hemangioma: A hospital-based prospective study

    • Authors: Jignaben Krunal Padhiyar, Nayan H Patel, Trusha P Gajjar, Mansi D Buch, Yogesh B Shah, Rekha Solanki
      Pages: 224 - 229
      Abstract: Jignaben Krunal Padhiyar, Nayan H Patel, Trusha P Gajjar, Mansi D Buch, Yogesh B Shah, Rekha Solanki
      Indian Journal of Paediatric Dermatology 2018 19(3):224-229
      Background: Propranolol may be more effective and safer than previously established therapies, and it may be used as a first-line therapy for infantile hemangioma (IH). Propranolol is thought to inhibit the growth of blood vessels by decreasing vascular endothelial growth factor. Aims and Objectives: The aim of this study is to study the efficacy and safety of propranolol in IH and for standardization of dose in tablet form. Materials and Methods: A total of 23 patients with 30 IH s were recruited in the study prospectively, after ruling out any contraindications for oral propranolol and obtaining consent from parents. Patients with <7 kg weight were given oral propranolol 5 mg twice daily and >7 kg weight were given 5 mg thrice daily. Patients were evaluated according to visual analog scale and ultrasonographically on day 0, day 30, day 60, and day 90. Results: Out of a total of 30, 25 (83.33%) were superficial, 3 (10%) were deep, and 2 (6.66%) were mixed hemangioma. All patients with superficial hemangiomas showed a change in the color of the lesion and arrest of growth within the 1st month of therapy and a gradual decrease in size was noticed in 23 (92%, n = 25) patients during the study period except in 2 (8%). Complete clearance was noticed in 68% of patients of superficial hemangioma at the end of the study period. Out of 25 patients, a total of 5 (20%) patients had ulceration at the time of presentation which started to heal within 15 days of therapy. Five (16.66%, n = 30) patients with deep and mixed variety showed arrest of growth but no decrease in size. No side effects were seen except temporary coldness of extremity in 1 (3.33%) patient. Conclusion: Propranolol is safe and effective for treatment of proliferative phase of superficial hemangiomas with very less side effects compared to oral steroids and other recommended therapies, and unavailability of syrup can be overcome by giving tablet in fixed dosage.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):224-229
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_75_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • The efficacy of a combination of oral low-dose prednisolone with
           propranolol for the treatment of infantile hemangioma

    • Authors: Pradyumna Pan
      Pages: 230 - 235
      Abstract: Pradyumna Pan
      Indian Journal of Paediatric Dermatology 2018 19(3):230-235
      Background: Infantile hemangiomas (IHs) are very common vascular tumors. Corticosteroid and propranolol are drugs for the treatment of hemangioma. High dose given for longer duration causes higher side effects. Aim and Objective: The aim and objective of this study was to determine the outcome of a combination of low-dose oral prednisolone with oral propranolol for the treatment of IH. Methods: The study comprised 42 consecutive patients with IH managed with low-dose oral prednisolone and oral propranolol between 2013 and 2016. Patients fulfilling the inclusion criteria were registered through the outpatient department. Diagnosis was confirmed clinically and on Color Doppler. All the patients were given oral prednisolone at a dose of 1 mg/kg/day and propranolol at a dose of 1.5 mg/kg/day. Treatment was given for 4 months and then titrated down for 2 months before the cessation of treatment. Results: Distribution was more on head, face, and neck. The median age at the start of treatment was 4.7 months. Out of the total 42 patients, forty patients responded to therapy (95.2%). Results were found to be excellent in 57.14% of infants and good in 30.95%. Treatment failure was seen in 4.7%. Side effects were not serious and resolved when treatment was discontinued. Rebound growth occurred in two infants (4.7%). No patients suffered drug morbidity. Conclusion: The frequency of acceptable outcome of a combination of low-dose oral prednisolone with oral propranolol for the treatment of IH shows high efficacy, low severe complication rate, and rapid clinical improvement.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):230-235
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_103_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Cutaneous manifestations of juvenile onset lupus erythematosus: A clinical
           study

    • Authors: Vinitha Panicker, Anil Mathew, Gopikrishnan Anjaneyan, Soumya Jagadeesan, S. Lekshmi, Jacob Thomas
      Pages: 236 - 240
      Abstract: Vinitha Panicker, Anil Mathew, Gopikrishnan Anjaneyan, Soumya Jagadeesan, S. Lekshmi, Jacob Thomas
      Indian Journal of Paediatric Dermatology 2018 19(3):236-240
      Introduction: Juvenile-onset systemic lupus erythematosus (SLE) is one of the most common systemic autoimmune connective tissue disorders in children. Studies focusing on the mucocutaneous manifestations of childhood lupus are scanty in literature. Objectives: This study was an attempt to describe the cutaneous changes seen in Pediatric Lupus and to correlate with the histopathological and immunofluoresecence findings. Methods: This was a retrospective study. All children under the age of 18 years who were diagnosed to have SLE according to the ACR criteria and presented to the dermatology outpatient department during a period of 1 year were included in the study. Details including clinical features, investigation findings including immunological tests and skin biopsy findings were noted. The analysis was performed using descriptive statistical tools such as percentage and frequency. Results: A total of 14 cases, average age at presentation was 10.14 years. Among the cutaneous manifestations, the most common presenting feature was urticarial vasculitis. Malar rash was seen in 57% of cases. Other cutaneous features seen were diffuse alopecia, oral ulcers. Antinuclear antibody was positive in all cases. Conclusion: Pediatric lupus tends to have a more aggressive course than adult lupus. Early diagnosis and treatment is necessary to prevent progression and development of complications.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):236-240
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_108_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • A novel case of chronic mucocutaneous candidiasis: Overlap between
           autoimmune polyendocrinopathy, candidiasis, ectodermal dystrophy syndrome
           and hyper IgE syndrome

    • Authors: Bauyelal Mahto, Payel Kundu, Aniruddha Ghosh, Sandipan Dhar
      Pages: 241 - 244
      Abstract: Bauyelal Mahto, Payel Kundu, Aniruddha Ghosh, Sandipan Dhar
      Indian Journal of Paediatric Dermatology 2018 19(3):241-244
      Chronic mucocutaneous candidiasis (CMC) is a clinical entity where extensive fungal infection of skin, hair, nail, and mucosa with Candida sp. is seen. It has got association with several immunological and endocrinal dysfunctions. We report a case of a 14-year-old boy who presented with peculiar facies, gross failure to thrive, fungal granulomatous lesions with scaring alopecia, oropharyngeal candidiasis, ectodermal dystrophy, grade 3 clubbing of all four limbs, interstitial keratitis with leukoma due to recurrent corneal ulcerations, and persistent deciduous teeth. A diagnosis of CMC was made and evaluation of immunological pathways revealed a high titer of immunoglobulin E. CMC with overlapping features of autoimmune polyendocrinopathy candidiasis ectodermal dystrophy syndrome and hyper IgE syndrome is extremely rare in literature. Timely diagnosis of an underlying etiology and proper treatment of a case of CMC may provide a better quality of life of the patient.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):241-244
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_20_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Homozygous familial hypercholesterolemia: A rare case report

    • Authors: Shashikant Malkud, Sirisha Varala, Geeta Kiran Arakkal, Purnachandra Badabagni
      Pages: 245 - 247
      Abstract: Shashikant Malkud, Sirisha Varala, Geeta Kiran Arakkal, Purnachandra Badabagni
      Indian Journal of Paediatric Dermatology 2018 19(3):245-247
      A 9-year-old male child presented with asymptomatic skin-colored-to-yellowish nodules over both the buttocks, feet, and over the right Achilles' tendon for 4 years. There was a history of similar complaints in elder sibling and also a history of premature sudden cardiac death in father. Biopsy from the lesions was suggestive of xanthoma. Fasting lipid profile was consistent with the pattern of Type IIa hyperlipoproteinemia. The child was further worked up for systemic involvement which was normal. He was started on rosuvastatin and fenofibrate and is under regular follow-up. The timely diagnosis of familial hypercholesterolemia, especially the homozygous variant, is important for early intervention and prevention of complications.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):245-247
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_47_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Chronic mucocutaneous candidiasis

    • Authors: Sarita Sasidharanpillai, Najeeba Riyaz, Nilambur K Supriya, Karumathil P Aravindan, Valiyaveettil Bindu, Muhammedkutty Simin, Geeta Govindaraj
      Pages: 248 - 250
      Abstract: Sarita Sasidharanpillai, Najeeba Riyaz, Nilambur K Supriya, Karumathil P Aravindan, Valiyaveettil Bindu, Muhammedkutty Simin, Geeta Govindaraj
      Indian Journal of Paediatric Dermatology 2018 19(3):248-250
      Chronic mucocutaneous candidiasis is a rare entity characterized by isolated defective immunity against candida infection. It manifests with resistant and relapsing superficial candida infection affecting skin, hair, nails, and mucosae. Although serious invasive disease is uncommon, this condition produces considerable morbidity in the affected. Long-term antifungal treatment is the preferred option. We report a 3½-year-old female child who presented with chronic mucocutaneous candidiasis and who showed a gradual response to long-term treatment with itraconazole.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):248-250
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_54_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • A boy with bird-like facies and ataxia: Cockayne syndrome

    • Authors: Vishalakshi S Pandit
      Pages: 251 - 254
      Abstract: Vishalakshi S Pandit
      Indian Journal of Paediatric Dermatology 2018 19(3):251-254
      Introduction: Congenital photosensitive disorders are a group disorders presenting with photosensitivity, short stature (SS), systemic manifestations and susceptibility to malignancy. These include Bloom syndrome, Cockayne syndrome (CS), Rothmund-Thompson syndrome, etc. Early identification and differentiating the syndrome from other congenital disorder is essential as the prognosis of each disorder differs. Case Report: A 4year-old-boy presented with photosensitive rash over the butterfly area of the face. He had history of delayed developmental milestones. His height and weight for his age were below the first percentile. On examination, patient had microcephaly, bird-like facies including sunken eyes, pinched nose, cachectic physique, ataxia and flexural contractures at elbow, knee and ankle joints. Ophthalmic examination showed pigmentary retinopathy on fundoscopy. CT scan of brain revealed bilateral basal ganglia calcification and evidence of premature mild cerebral atrophic changes. On the basis of clinical and lab investigations, we diagnosed this case as CS. Discussion: CS is a rare AR disorder characterized by normal prenatal growth with the onset of growth and developmental abnormalities in the first two years. They have SS, sexual immaturity, and/or retinal pigmentation. Diagnosis of the CS is made by characteristic clinical features specific to this, but the definitive diagnosis is achieved by laboratory investigations such as cytogenetic, biochemical and molecular methods. Although there is no specific treatment, avoidance of sun exposure and protection by sunscreens can help prevent some of the cutaneous eruptions associated with photosensitivity.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):251-254
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_83_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Mimicker of perianal papular lesions

    • Authors: Ebtisam Elghblawi
      Pages: 255 - 257
      Abstract: Ebtisam Elghblawi
      Indian Journal of Paediatric Dermatology 2018 19(3):255-257
      Perianal mimicker papular skin lesion in children is rare when the real cause cannot be found or justified. I report a young 4-year-old black Libyan girl who complaint of multiple itchy skin-colored nodules for the past 1 year around only the anus and increasing as her mother declared. Cutaneous examination revealed multiple, 0.5–1 cm flat-topped dry papules, at the perianal area not extending up to the labia majora. On histology marked focal epidermal hyperplasia and hyperkeratosis in the epidermis was seen. This confirmed the diagnosis of one condition stated in the literature called perianal pseudoverrucous papules and nodule. This rare condition can be mistaken with sexually transmitted diseases leading to unnecessary investigations and treatment and raising the question of sexual abuse in children.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):255-257
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_43_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Solitary mastocytoma arising from a tight infant identification bracelet

    • Authors: Wei-Liang Koh, Yong-Kwang Tay, Chee-Seng Sim
      Pages: 258 - 260
      Abstract: Wei-Liang Koh, Yong-Kwang Tay, Chee-Seng Sim
      Indian Journal of Paediatric Dermatology 2018 19(3):258-260
      Mastocytosis is characterized by a proliferation of mast cells in the skin and extracutaneous organs. Cutaneous mastocytoma is the second most common presentation of mastocytosis in children and has been reported to arise post-trauma. We report herein the second case of solitary mastocytoma resulting from application of an excessively tight infant identification bracelet and the first in the English literature.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):258-260
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_85_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Pachyonychia congenita: Affecting three generations!

    • Authors: Rohit Singla, Pihu Sethi, TG Savitha, Amrinder Jit Kanwar
      Pages: 261 - 262
      Abstract: Rohit Singla, Pihu Sethi, TG Savitha, Amrinder Jit Kanwar
      Indian Journal of Paediatric Dermatology 2018 19(3):261-262
      Pachyonychia congenita is an autosomal dominantly inherited disease that primarily presents as nail dystrophy and dyskeratosis of skin and mucous membranes. A 32-year-old female presented with thickening of the nails and thickening of both heels. Her father showed pincer nails with periungual thickening of skin and fissures with focal plantar keratoderma. Her two sons had similar nail changes.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):261-262
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_11_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • A child with multiple café au lait macules: Rare presentation of
           plexiform neurofibromatosis with facial dysmorphism, alopecia, proptosis,
           stridor, and limb length discrepancy

    • Authors: Aniruddha Ghosh, Payel Kundu, Sandipan Dhar, Arunaloke Bhattacharya
      Pages: 263 - 265
      Abstract: Aniruddha Ghosh, Payel Kundu, Sandipan Dhar, Arunaloke Bhattacharya
      Indian Journal of Paediatric Dermatology 2018 19(3):263-265
      Multiple café au lait macules are one of the cornerstones in diagnosing neurofibromatosis Type 1 (NF 1). NF 1 is often a multisystem neurocutaneous disorder, plexiform NF being one of the most important variants of this phacomatosis. Here, a rare case of a 2.5-year-old male child without positive family history has been described who presented with multiple large café au lait spots, alopecia, dysmorphic facies, proptosis, protrusion and deviation of tongue, biphasic stridor, bilateral neck swelling, and abnormal gait due to foreshortened left leg. Magnetic resonance imaging revealed abnormal soft-tissue infiltration of cavernous sinus through sphenoid bone, retro-orbital, retropharyngeal, parapharyngeal spaces, floor of mouth, and encasement of unilateral neck vessels and compression over trachea. Indirect laryngoscopy revealed unilateral vocal cord palsy most likely due to recurrent laryngeal nerve involvement. Biopsy confirmed the diagnosis of NF. Pediatricians and dermatologists should be aware of syndromic causes and their varied presentations while encountering a child with multiple large café au lait spots.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):263-265
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_12_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Systematized inflammatory linear verrucous epidermal nevus moderately
           responsive to systemic acitretin and topical calcipotriol

    • Authors: Sanjay Singh, Mamta Rai, Neetu Bhari, Savita Yadav
      Pages: 266 - 268
      Abstract: Sanjay Singh, Mamta Rai, Neetu Bhari, Savita Yadav
      Indian Journal of Paediatric Dermatology 2018 19(3):266-268
      Inflammatory linear verrucous epidermal nevus (ILVEN) is a rare form of epidermal nevus which usually presents in childhood, mostly on the lower half of the body in a blaschkoid distribution. A wide variety of topical, systemic, and surgical modalities have been tried for its treatment, but it is known to be refractory to treatment. We hereby are reporting a rare case of extensive systematized ILVEN which showed moderate response to treatment with acitretin and topical calcipotriol.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):266-268
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_53_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Extensive childhood alopecia areata responding to combination of oral
           cyclosporine and corticosteroid therapy – clinical experience in
           four patients

    • Authors: Nibedita Patro, Maitreyee Panda, Sibasish Patro, Madhuchhanda Mohapatra
      Pages: 269 - 271
      Abstract: Nibedita Patro, Maitreyee Panda, Sibasish Patro, Madhuchhanda Mohapatra
      Indian Journal of Paediatric Dermatology 2018 19(3):269-271
      Alopecia areata (AA) is a disease of unpredictable treatment outcome. Due to a great psychosocial impact associated with the disease, multitudes of therapy have been tried. We recommend safe consideration of oral cyclosporine in cases of extensive nonresponsive childhood AA.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):269-271
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_60_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Focal actinic porokeratosis: A new variant?

    • Authors: Pihu Sethi, Neeti Kumari, Bhuvan Adhlakha, Amrinder Jit Kanwar
      Pages: 272 - 273
      Abstract: Pihu Sethi, Neeti Kumari, Bhuvan Adhlakha, Amrinder Jit Kanwar
      Indian Journal of Paediatric Dermatology 2018 19(3):272-273
      Porokeratosis is an autosomal dominantly transmitted disorder of keratinization predominantly affecting trunk and extremities. Many clinical variants have been described having a common histopathological feature of coronoid lamella-porokeratosis of Mibelli, superficial disseminate, disseminated superficial actinic porokeratosis, linear porokeratosis and punctuate palmoplantar porokeratosis. We present a case of 16-year-old female who had focal lesions of porokeratosis aggravated by sun exposure, over alae of nose confirmed by histopathology. The previous reports show quite a number of cases of isolated lesions of the disease on nose and perinasal area. This article highlights the actinic nature of focal facial porokeratosis.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):272-273
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_9_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Autosomal recessive cutis laxa type-1 with complex systemic manifestations

    • Authors: Shruti Dhanraj Chavan, Ashish Ramchandra Deshmukh, Aniruddha Dharnidhar Gulanikar, Shilpa Satyajeet Pathrikar, Iqbal Mohammad Tariq
      Pages: 274 - 276
      Abstract: Shruti Dhanraj Chavan, Ashish Ramchandra Deshmukh, Aniruddha Dharnidhar Gulanikar, Shilpa Satyajeet Pathrikar, Iqbal Mohammad Tariq
      Indian Journal of Paediatric Dermatology 2018 19(3):274-276
      Cutis laxa (CL) is a rare connective tissue disorder characterized by loose, sagging, and redundant skin. Both inherited and acquired forms are known. A 7-year-old boy, presented with loose, sagging skin chiefly over the face, extremities, and skin folds since birth with recurrent respiratory and systemic complaints. The patient had a characteristic senile bloodhound appearance. Chest X-ray findings included emphysema, bronchopneumonia, and pulmonary hypertension. Ultrasonographic examination showed cystitis and bladder diverticula. Two-dimensional echocardiography showed primary pulmonary hypertension. Histopathological examination with Verhoeff-Van-Gieson stain showed markedly reduced elastic fibers. Serum amino acids, copper, and ceruloplasmin were normal. About sixty cases of autosomal recessive cutis laxa type 1 (ARCL-1) have been reported in literature. There is no definitive treatment available at present, and symptomatic management is the mainstay of treatment. Differential diagnosis includes Ehlers–Danlos syndrome, congenital disorders of glycosylation syndrome, and pseudoxanthoma elasticum. We report this case of ARCL-1 for its rarity and complex systemic involvement.
      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):274-276
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_65_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Darier&#39;s sign

    • Authors: Tarang Goyal, Sakshi Kohli
      Pages: 277 - 279
      Abstract: Tarang Goyal, Sakshi Kohli
      Indian Journal of Paediatric Dermatology 2018 19(3):277-279

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):277-279
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_61_18
      Issue No: Vol. 19, No. 3 (2018)
       
  • Hot topics in pediatric dermatology

    • Authors: Rajsmita Bhattacharjee, Rahul Mahajan
      Pages: 280 - 284
      Abstract: Rajsmita Bhattacharjee, Rahul Mahajan
      Indian Journal of Paediatric Dermatology 2018 19(3):280-284

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):280-284
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_64_18
      Issue No: Vol. 19, No. 3 (2018)
       
  • Severe acute malnutrition with hyperpigmentation: An uncommon association

    • Authors: Ibrahim Aliyu, Zainab F Ibrahim
      Pages: 285 - 286
      Abstract: Ibrahim Aliyu, Zainab F Ibrahim
      Indian Journal of Paediatric Dermatology 2018 19(3):285-286

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):285-286
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_25_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Atypical dermatological manifestation of neonatal chikungunya

    • Authors: Amitabh Singh, Anirban Mandal
      Pages: 286 - 287
      Abstract: Amitabh Singh, Anirban Mandal
      Indian Journal of Paediatric Dermatology 2018 19(3):286-287

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):286-287
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_46_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • LEOPARD syndrome with late onset lentigines: A rarity

    • Authors: Sunder Nagakeerthana, Sankar Madhavi, Kaliaperumal Karthikeyan
      Pages: 287 - 290
      Abstract: Sunder Nagakeerthana, Sankar Madhavi, Kaliaperumal Karthikeyan
      Indian Journal of Paediatric Dermatology 2018 19(3):287-290

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):287-290
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_4_17
      Issue No: Vol. 19, No. 3 (2018)
       
  • Bilateral nevus of ota with involvement of palate: A rare case report

    • Authors: Mohammad Adil, Syed Suhail Amin, Dinesh Raj, Mahtab Alam
      Pages: 290 - 292
      Abstract: Mohammad Adil, Syed Suhail Amin, Dinesh Raj, Mahtab Alam
      Indian Journal of Paediatric Dermatology 2018 19(3):290-292

      Citation: Indian Journal of Paediatric Dermatology 2018 19(3):290-292
      PubDate: Thu,28 Jun 2018
      DOI: 10.4103/ijpd.IJPD_97_17
      Issue No: Vol. 19, No. 3 (2018)
       
 
 
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