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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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| Published in: | Med Genet |
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| Main Authors: | , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Springer Medizin
2018
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5838123/ https://ncbi.nlm.nih.gov/pubmed/29527097 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11825-018-0173-7 |
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