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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 least 1 out of 4500 w...

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Bibliografische gegevens
Hoofdauteurs: Camborieux Laure, Morcel Karine, Guerrier Daniel
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMC 2007-03-01
Reeks:Orphanet Journal of Rare Diseases
Online toegang:http://www.OJRD.com/content/2/1/13
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