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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2007-03-01
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Series: | Orphanet Journal of Rare Diseases |
Online Access: | http://www.OJRD.com/content/2/1/13 |