Mayer-Rokitansky-Küster-Hauser syndrome associated with 7q11.23 microduplication: A case report
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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. ... ...