Ring chromosome 11

Ring chromosome 11 syndrome is an autosomal anomaly characterized by variable clinical features, including early growth retardation and short stature, microcephaly, developmental delay, some degree of intellectual disability, facial dysmorphism and café-au-lait spots. In some cases, congenital heart disease and endocrine abnormalities have been reported.

Also known as: RC11, Ring chromosome type 11, r(11) syndrome, Ring 11, Ring chromosome 11 syndrome, chromosome 11 ring, r11

2 clinical trials for this condition and its sub-types.