后肠和下尿路完全重复并伴有双阴茎。
Complete duplication of the hindgut and lower urinary tract with diphallus.
作者信息
Azmy A F
机构信息
Department of Paediatric Surgery, Royal Hospital for Sick Children, Glasgow, Scotland.
出版信息
J Pediatr Surg. 1990 Jun;25(6):647-9. doi: 10.1016/0022-3468(90)90355-d.
PMID:2359002
Abstract
An infant is reported with complete duplication of the colon, rectum, anus, terminal ileum up to the point of Meckel's diverticulum, doubling of the genitalia with completely formed penes, double bladder and urethra, multiple spinal anomalies, omphalocele, and large lower abdominal wall hernia with wide separation of the symphysis pubis.
摘要
据报道，一名婴儿出现结肠、直肠、肛门、直至梅克尔憩室处的回肠末端完全重复，生殖器双倍发育且阴茎完全形成，膀胱和尿道双份，多种脊柱异常，脐膨出，以及耻骨联合分离的巨大下腹壁疝。
Zotero 插件