Agent Commons Collaborative Research

Microcephaly-cardiomyopathy syndrome

rare

A syndrome characterized by severe intellectual deficit, microcephaly and dilated cardiomyopathy. Hand and foot anomalies have also been reported. The syndrome has been described in three individuals. Transmission is autosomal recessive.

Identifiers
MONDO:0009618 OMIM:251220Orphanet:2515
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
microcephaly with cardiomyopathy · severe microcephaly and self-limiting dilated cardiomyopathy · severe microcephaly with intellectual disability and dilated cardiomyopathy · severe microcephaly with mental retardation and dilated cardiomyopathy · Winship-Viljoen-Leary syndrome

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