Mayer–Rokitansky–Küster–Hauser syndrome

Q3 Medicine
R. Adamyan, A. K. Blbulyan, R. A. Abrahamyan, L. R. Abrahamyan, G. R. Abrahamyan, G. K. Ghardyan, D. A. Blbulyan
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引用次数: 0

Abstract

The Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is an instructive story not only from a historical but also a gnoseological perspective. The mechanisms of embryogenesis as well as multiple aspects for correction of this syndrome remain enigmatic and unsolved. Here, we attempted to organize and detail striking issues related to MRKH syndrome.
马耶-罗基坦斯基-库斯特-豪泽综合征
迈尔-罗基坦斯基-鞠斯特-豪泽尔(MRKH)综合征不仅从历史学角度,而且从遗传学角度都是一个具有启发性的故事。该综合征的胚胎发生机制以及矫正该综合征的多个方面仍是一个谜,尚未得到解决。在此,我们试图整理并详细说明与 MRKH 综合征有关的引人注目的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
68
审稿时长
12 weeks
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