X-linked intellectual disability-ataxia-apraxia syndrome

Orpha code: 85338OMIM code:

Definicja

A rare, X-linked syndromic intellectual disability disorder characterized by non-progressive ataxia, apraxia, variable intellectual disability and/or visuospatial, visuographic and visuoconstructive dysfunctions in male patients. Seizures, congenital clubfoot and macroorchidism have also been associated. Partial clinical expression was noted in obligate female carriers. There have been no further descriptions in the literature since 1992.

Disease data
Klasyfikacja

Disease

Kod ORPHA
85338
Kod OMIM
-
Kod ICD10
G31.8
Kod ICD11
-

No additional description.

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