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Синдром ектодермальної дисплазії - сліпоти

ORPHA:1806· ICD-10 Q87.8· Ectodermal dysplasia-blindness syndrome

Визначення(English summary)

A rare multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, severe visual impairment due to ocular malformations (microphthalmos and microcornea with sclerocornea), short stature, hypotrichosis, dental anomalies, and dysmorphic facial features (such as a narrow nasal bridge with marked distal flaring and low-set, protruding ears). There have been no further descriptions in the literature since 1992.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Neonatal