罕见的子宫畸形。双宫颈单子宫体及单阴道。
Unusual uterine malformation. Double cervix with single corpus and single vagina.
作者信息
Tavassoli F
出版信息
Obstet Gynecol. 1977 Mar;49(3):366-9.
PMID:840467
Abstract
An unusual uterine malformation in which double cervix was the sole müllerian tube fusion defect is presented. It was associated with numerous other congenital anomalies in a 4-month-old infant with normal chromosome studies. The embryologic significance of this defective fusion is discussed.
摘要
本文报道了一例罕见的子宫畸形，其中双宫颈是唯一的苗勒管融合缺陷。该病例发生在一名4个月大的婴儿身上，除上述畸形外还伴有许多其他先天性异常，但其染色体检查结果正常。本文还讨论了这种融合缺陷的胚胎学意义。
Zotero 插件