先天性短结肠症属于小儿肠道发育中罕见的畸形，查阅国内有关文献资料，报道仅１０余例，该病多合并其他畸形，如先天性肛门闭锁、直肠阴道瘘、先天性巨结肠等，本例除合并以上畸形外，同时合并先天性双子宫及双阴道，临床更为罕见，特报道如下。患儿，女，２月。出生后发现无? Congenital short-bowel disease is a rare deformity in children with intestinal development, access to domestic literature, reported only more than 10 cases, the disease combined with other malformations, such as congenital anal atresia, rectovaginal fistula, Hirschsprung etc., In addition to the above cases in addition to deformity, concomitant congenital double uterus and double vagina, the more common clinical, reported as follows. Children, women, February. Not found after birth?