This syndrome has characteristics of intellectual and motor deficit, spastic quadriparesis and agenesis of the corpus callosum, without craniofacial abnormalities or seizures. It has been described in four male members of a family. The mode of inheritance is most likely X-linked recessive.
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No extended properties.
Concept Alternate Designations
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Concept Designation Description
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Code Flag
3315137014
X-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome