Aniridia-intellectual disability syndrome

Orpha code: 1068OMIM code:

Definition

An extremely rare autosomal dominant developmental defect of the eye described in several members of one family that is characterized by the association of moderate intellectual disability with aniridia, lens dislocation, optic nerve hypoplasia and cataracts. There have been no further descriptions in the literature since 1974.

Disease data
Classification

Malformation syndrome

Synonyms
Walker-Dyson syndrome
Zespół Walkera i Dysona
ORPHA code
1068
OMIM code
-
ICD10 code
Q13.1
ICD11 code
-

No additional description.

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