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Clinical and genetic aspects of Mayer–Rokitansky–Küster–Hauser syndrome
The Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome [MIM 277000] is characterised by the absence of a uterus and vagina in otherwise phenotypically normal women with karyotype 46,XX. Clinically, the MRKH can be subdivided into two subtypes: an isolated or type I form can be delineated from a type II...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Medizin
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838123/ https://www.ncbi.nlm.nih.gov/pubmed/29527097 http://dx.doi.org/10.1007/s11825-018-0173-7 |