The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of 4500 women and has for a long time been considered as a sporadic anomaly. Congenital absence of upper vagina and uterus is the prime feature of the disease which, in addition, is often found associated with unilateral renal...

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Detalles Bibliográficos
Autores principales: Guerrier, Daniel, Mouchel, Thomas, Pasquier, Laurent, Pellerin, Isabelle
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Mini-Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1368996/
https://www.ncbi.nlm.nih.gov/pubmed/16441882
http://dx.doi.org/10.1186/1477-5751-5-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1368996/
https://www.ncbi.nlm.nih.gov/pubmed/16441882
http://dx.doi.org/10.1186/1477-5751-5-1

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