Ectodermal dysplasia-blindness syndrome

Orpha code: 1806OMIM code: 268320

Definition

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
Classification

Malformation syndrome

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

No additional description.

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