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Introduction
Mayer‐Rokitansky‐Küster‐Hauser syndrome (MRKHS) is characterized by congenital absence of the uterus and the upper two‐thirds of the vagina in otherwise phenotypically normal females. It is found isolated or associated with renal, skeletal and other malformations. Despite ongoing research, the etiology is mainly unknown. For a long time, the hypothesis of deficient hormone receptors...
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