X-linked intellectual disability-ataxia-apraxia syndrome

Orpha code: 85338OMIM code:

Definition

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
Classification

Disease

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

No additional description.

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