Ectodermal dysplasia-blindness syndrome

Orpha code: 1806OMIM code: 268320

Definicja

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.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
1806
Kod OMIM
268320
Kod ICD10
Q87.8
Kod ICD11
LD27.0Y

No additional description.

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