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Синдром пізнього локалізованого бульозного епідермолізу та інтелектуальної недостатності

ORPHA:231556· ICD-10 Q81.8· Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome

Визначення(English summary)

A rare junctional epidermolysis bullosa subtype characterized by late-onset blistering surrounded by erythema and localized on the anterior aspect of the lower legs, associated with dystrophic toenails, tooth enamel defects and mild to severe intellectual disability. Lens subluxation and mild facial dysmorphism (with short midface, prognatism and thin upper lip vermilion) are additional reported features. There have been no further descriptions in the literature since 1992.

Поширеність
<1 / 1 000 000
Успадкування
Unknown
Вік початку
Childhood