Bartsch O, Kuhnle U, Wu L L, Schwinger E, Hinkel G K
Institute of Clinical Genetics, University Hospital Carl Gustav Carus, Technical University Dresden, Germany.
Am J Med Genet. 1996 Oct 28;65(3):218-21. doi: 10.1002/(SICI)1096-8628(19961028)65:3<218::AID-AJMG9>3.0.CO;2-L.
Two unrelated patients with small distal deletions of the long arm of chromosome 13 are described, with shawl scrotum and penoscrotal transposition, penoscrotal hypospadias, a reduced perineum, and anal atresia. The patients have small deletions of 13(q32.2qter) and 13(q32q34), respectively. This report and the literature present evidence for one or possibly more gene(s) within region 13q32.2q34 which regulate the development of the ano-genital structures. The clinical spectrum includes bifid or shawl scrotum, hypospadias, biseptate uterus, malplaced and imperforate anus, and common cloaca.
本文描述了两名患有13号染色体长臂远端小缺失的无关患者,他们存在阴囊垂挂和阴茎阴囊转位、阴茎阴囊型尿道下裂、会阴缩小以及肛门闭锁。两名患者分别有13(q32.2qter)和13(q32q34)的小缺失。本报告及文献表明,13q32.2q34区域内存在一个或可能多个调控肛门生殖器结构发育的基因。临床谱系包括双裂或阴囊垂挂、尿道下裂、双子宫、肛门异位和闭锁以及泄殖腔畸形。