Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.

@article{Oppelt2006ClinicalAO,
  title={Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.},
  author={Peter Oppelt and Stefan Peter Renner and Anja Kellermann and Sara Brucker and Georges A Hauser and Kurt S. Ludwig and Pamela L. Strissel and Reiner Strick and Diethelm Wallwiener and Matthias W. Beckmann},
  journal={Human reproduction},
  year={2006},
  volume={21 3},
  pages={792-7}
}
BACKGROUND The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is a malformation of the female genitals (occurring in one in 4000 female live births) as a result of interrupted embryonic development of the Müllerian (paramesonephric) ducts. This retrospective study examined the issue of associated malformations, subtyping, and the frequency distribution of subtypes in MRKH syndrome. METHODS Fifty-three MRKH patients were investigated using a newly developed standardized questionnaire… CONTINUE READING
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