Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

<p>Abstract</p> <p>The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. It affects at lea...

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Bibliographic Details
Main Authors: Camborieux Laure, Morcel Karine, Guerrier Daniel
Format: Article
Language:English
Published: BMC 2007-03-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.OJRD.com/content/2/1/13