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Vaginal agenesis (mayer - rokitansky - küster - hauser syndrome): recent etiopathogenetical and anatomical views.

作者信息

Ghirardini G, Segre A

出版信息

Clin Exp Obstet Gynecol. 1982;9(2):98-102.

PMID:6761012
Abstract

Congenital absence of uterus and vagina is a picture known as Mayer-Rokitansky-Küster-Hauser syndrome. Six cases are reported and particular attention is devoted to the anatomical pictures, which can be found in typical or atypical form. Discussion on the etiopathogenetical problems, supporting Hauser's hypothesis of an inhibition of the müllerian ducts development by MIF production, allows to consider it as the slightest form of female pseudoermaphroditism. Moreover the terms used to delineate this condition, like "müllerian aplasia", "müllerian ducts aplasia", "müllerian ducts agenesis" and "uterovaginal agenesis" may be misleading and the term of "müllerian dysgenesis syndrome" is proposed.

摘要

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引用本文的文献

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Mayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment.梅耶-罗基坦斯基-库斯特-豪泽综合征:胚胎学、遗传学以及临床与外科治疗
ISRN Obstet Gynecol. 2013;2013:628717. doi: 10.1155/2013/628717. Epub 2013 Feb 4.
2
Spinal abnormalities and the atypical form of the Mayer-Rokitansky-Küster-Hauser syndrome.脊柱异常与 Mayer-Rokitansky-Küster-Hauser 综合征的非典型形式
Skeletal Radiol. 1992;21(7):459-62. doi: 10.1007/BF00190992.