2) müllerian duct syndrome
苗勒管综合征
3) incomplete Mllerian fusion
苗勒管融合不全
1.
Methods: HOXA13 gene was detected in 58 Chinese Han patients(including 51 patients with incomplete Mllerian fusion, 7 congenital absence of uterus and vagina (CAUV)) and 54 control individuals.
方法:对58例中国汉族苗勒管发育异常患者(包括51例苗勒管融合不全患者、7例先天性无阴道无子宫患者)和54例正常对照者进行HOXA13基因检测。
4) Cleidocranial dysplasia(CCD)
颅锁骨发育不全综合征
5) Testicular dysgenesis syndrome(J Reprod Med2008,17(2):146-150)
睾丸发育不全综合征
6) persistent Müllerian duct syndrome
苗勒管永存综合征
1.
Objective:To study the etiopathogenesis,clinical manifestations,diagnosis and management of persistent Müllerian duct syndrome(PMDS).
目的:探讨苗勒管永存综合征(PMDS)的病因、临床表现、诊断和治疗。
补充资料:巴彻勒氏综合征