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10.2147/IJWH.S75637

http://scihub22266oqcxt.onion/10.2147/IJWH.S75637
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C4636170!4636170!26586965
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suck abstract from ncbi

pmid26586965      Int+J+Womens+Health 2015 ; 7 (ä): 865-70
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  • Mayer-Rokitansky-Kuster-Hauser syndrome: a review #MMPMID26586965
  • Londra L; Chuong FS; Kolp L
  • Int J Womens Health 2015[]; 7 (ä): 865-70 PMID26586965show ga
  • The congenital aplasia or severe hypoplasia of mullerian structures is infrequent. However, the features of normal female endocrine function paired with the absence of a functional uterus and vagina makes it a fascinating entity. The diagnosis and work-up in these patients has become very efficient, thanks to the use of imaging, and there are multiple successful procedures for the creation of a neovagina. In recent years, infertility treatment options through in vitro fertilization have also become available as part of the long-term care of these patients.
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