vitalwiki

Дистрофічний бульозний епідермоліз

ORPHA:303· ICD-10 Q81.2· Dystrophic epidermolysis bullosa

Визначення(English summary)

A group of inherited epidermolysis bullosa (EB) characterized by cutaneous and mucosal fragility resulting in blisters and superficial ulcerations that develop below the lamina densa of the cutaneous basement membrane and that heal with significant scarring and milia formation. Dystrophic epidermolysis bullosa (DEB) comprises four major and several rare sub-types with the three most common being intermediate dominant DEB, severe recessive DEB and intermediate recessive DEB.

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