Microcephaly-Cardiomyopathy Syndrome
摘要
In 1991, Winship et al. reported a brother and sister from an unrelated Afrikaner couple. They had significant microcephaly with intellectual disability and dilated cardiomyopathy, which manifested in infancy (Figs. 1 and 2). Hand and foot anomalies, such as clinodactyly of the fifth finger on both hands and sandal gaps on both feet, were mentioned (Winship et al. 1991).