Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

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 women. MRKH may be i...

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Detalles Bibliográficos
Autores principales: Morcel, Karine, Camborieux, Laure, Guerrier, Daniel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1832178/
https://www.ncbi.nlm.nih.gov/pubmed/17359527
http://dx.doi.org/10.1186/1750-1172-2-13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1832178/
https://www.ncbi.nlm.nih.gov/pubmed/17359527
http://dx.doi.org/10.1186/1750-1172-2-13

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