Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome

Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterized by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopaenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15).

Also known as: ATRUS syndrome, RUSAT, radioulnar synostosis with amegakaryocytic thrombocytopenia

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