Baxová A, Maroteaux P, Barosová J, Netriová I
Department of Clinical Genetics, Dérerova nemocniaca, Bratislava, Slovakia.
Am J Med Genet. 1994 Feb 1;49(3):263-5. doi: 10.1002/ajmg.1320490303.
Two sibs with omodysplasia were born to phenotypically normal but consanguineous parents. They had severe micromelic dwarfism, facial anomalies, and mental retardation. One had a congenital heart defect. The radiographic findings are typical: hypoplastic distal end of the humerus with radioulnar diastasis. Parental consanguinity and clinical manifestations in 2 sibs suggest autosomal recessive inheritance.
两名患有短肢侏儒症的同胞兄弟姐妹出生于表型正常但为近亲结婚的父母。他们患有严重的短肢侏儒症、面部畸形和智力发育迟缓。其中一人患有先天性心脏缺陷。影像学表现典型:肱骨远端发育不全伴桡尺骨分离。父母近亲结婚以及两名同胞兄弟姐妹的临床表现提示为常染色体隐性遗传。