Mayer-Rokitansky-Küster-Hauser syndrome associated with 7q11.23 microduplication: A case report
Introduction: Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is characterized by the congenital absence of the uterus and vagina in females with 46, XX karyotype. The genetic etiology remains poorly understood. Case presentation: We described a 29-year-old female patient with a main complaint of pr...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
KeAi Communications Co., Ltd.
2025-06-01
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| Col·lecció: | Global Medical Genetics |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S2699940425000402 |
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