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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
PMID26586965
show 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.