先天性无阴道伴双始基子宫1例报告
Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome with Double Primordial Uterus: A Case Report
摘要:
先天性无阴道综合征是一种罕见的先天性女性生殖器官畸形疾病，发病率低，多数患者无阴道或仅存阴道盲端、子宫缺如或存在始基子宫或痕迹子宫，关于该病的研究较少。本文对1例先天性无阴道伴双始基子宫进行个案报道。
Abstract:
Mayer-Rokitansky-Küster-Hauser (MRKH) is a rare congenital malformation of female reproductive organs, with a low incidence. Most patients have no vagina or only vaginal blind end, absence of uterus or presence of primordial uterus or traces of uterus. There is less research on disease. This article reports a case of MRKH with double primordial uterus.
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