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. The disease is microcephaly-cardiomyopathy syndrome (Monarch Disease Ontology id MONDO_0009618). Also known as: Winship-Viljoen-Leary syndrome.