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X-linked intellectual disability-ataxia-apraxia syndrome

ORPHA:85338· ICD-10 G31.8

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.

Prevalence
<1 / 1 000 000
Inheritance
X-linked recessive
Age of onset
Childhood