Autosomal recessive nonsyndromic mental retardation-18

An autosomal recessive condition caused by mutation(s) in the CRADD gene, encoding death domain-containing protein CRADD. It is characterized by mild to moderate intellectual disability and lissencephaly with anterior-predominant pachygyria.

Disease Alternative Name

mental retardation
autosomal recessive 34
with variant lissencephaly
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