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Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
rareRadio-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).
- Identifiers
- MONDO:0011555 Orphanet:71289
- Part of
- Congenital hematological disorderCongenital limb malformationDysostosisSyndromic constitutional thrombocytopenia
- Also known as
- ATRUS syndrome · radioulnar synostosis with amegakaryocytic thrombocytopenia · RUSAT
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