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A classical variant of ectodermal dysplasia: a case report.
Switi Jawade1, Pratibha Wankhede2, Ranjana Sharma3
1Department of Obstetrics and Gynecology Nursing, Shalinitai Meghe College of Nursing, Salod (Hirapur), Datta Meghe Institute of Higher Education and Research (Deemed to be University), Sawangi, Wardha, Maharashtra, India.
The Pan African Medical Journal
|January 12, 2026
Summary
Ectodermal dysplasia, a rare congenital disorder affecting hair, nails, and sweat glands, presents diagnostic challenges, especially in children. This case highlights the evaluation and management of a sporadic presentation in a 10-year-old boy.
Area of Science:
- Genetics and Developmental Biology
- Pediatric Medicine
- Dermatology
Background:
- Ectodermal dysplasias (EDs) are rare congenital disorders affecting ectodermal structures like hair, nails, and sweat glands.
- Characterized by hypohidrosis, hypotrichosis, and hypodontia, EDs exhibit variable phenotypes, complicating pediatric diagnosis.
- Sporadic presentations are uncommon and pose significant diagnostic challenges.
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