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Bookmark or Share- Müllerian agenesis - WikipediaMüllerian agenesis, also known as Müllerian aplasia, vaginal agenesis, or Mayer–Rokitansky–Küster–Hauser syndrome (MRKH syndrome), is a congenital malformation characterized by a failure of the Müllerian ducts to develop, resulting in a missing uterus and variable degrees of vaginal hypoplasia of its upper portion.
- MRKH Syndrome | Symptoms, Diagnosis & Treatment - Cincinnati Children's ...Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome — also known as Müllerian agenesis or vaginal agenesis — is a rare condition that causes underdevelopment of the uterus, cervix and upper vagina. MRKH patients are born with this condition (congenital), which is diagnosed in childhood or adolescence.
- Mayer-Rokitansky-Küster-Hauser Syndrome - Cleveland ClinicWhat is Mayer-Rokitansky-Küster-Hauser syndrome? Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is a rare congenital disorder that can affect women and people assigned female at birth (AFAB). It’s a condition that causes your vagina and uterus to be missing or underformed.
- Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome - Penn MedicineWhat Is Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome? Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome is a rare congenital disorder that affects the female reproductive system. This condition is characterized by an underdeveloped vagina and uterus.
- Mayer-Rokitansky-Küster-Hauser syndrome - MedlinePlusMayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a disorder that mainly affects the female reproductive system. This condition causes the vagina and uterus to be underdeveloped or absent, although external genitalia are normal.
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