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Епідермолітична долонно-підошвова кератодермія

ORPHA:2199· ICD-10 Q82.8· Epidermolytic palmoplantar keratoderma

Визначення(English summary)

A rare, non-syndromic, hereditary palmoplantar keratoderma characterized by diffuse, yellowish, thick hyperkeratosis of the palms and soles with a sharp demarcation at the volar border and an erythematous margin, and the epidermolytic pattern of changes on the skin biopsy, including perinuclear vacuolization, granular degeneration of keratinocytes in the spinous and granular layer, and tonofilament aggregates. Painful fissures and hyperhidrosis are frequently associated.

Поширеність
1-9 / 100 000
Успадкування
Autosomal dominant
Вік початку
Infancy, Neonatal