Microcephaly-cardiomyopathy syndrome
MONDO:0009618A 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.
Also known as: Winship-Viljoen-Leary syndrome, microcephaly with cardiomyopathy, microcephaly-cardiomyopathy, severe microcephaly and self-limiting dilated cardiomyopathy, severe microcephaly with intellectual disability and dilated cardiomyopathy, severe microcephaly with mental retardation and dilated cardiomyopathy
0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly-cardiomyopathy syndrome itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.