Autosomal dominant palmoplantar keratoderma and congenital alopecia
ORPHA:1010· ICD-10 Q82.8
Definition
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- Infancy, Neonatal