A Cohort of 469 Mayer–Rokitansky–Küster–Hauser Syndrome Patients—Associated Malformations, Syndromes, and Heterogeneity of the Phenotype

A Cohort of 469 Mayer–Rokitansky–Küster–Hauser Syndrome Patients—Associated Malformations, Syndromes, and Heterogeneity of the Phenotype

The Mayer–Rokitansky–Küster–Hauser syndrome is characterized by aplasia of the uterus and upper two-thirds of the vagina. While it can appear as an isolated genital malformation, it is often associated with extragenital abnormalities, with little still known about the pathogenetic background. To pro...

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Bibliographic Details
Main Authors: Martin Pietzsch, Birgitt Schönfisch, Alice Höller, André Koch, Annette Staebler, Katharina Dreser, Kristina Bettecken, Lisa Schaak, Sara Yvonne Brucker, Katharina Rall
Format: Article
Language:English
Published: MDPI AG 2024-01-01
Series:Journal of Clinical Medicine
Subjects:
Mayer–Rokitansky–Küster–Hauser syndrome
MRKHS
uterine rudiments
uterine aplasia
vaginal aplasia
endometrial tissue
Online Access:https://www.mdpi.com/2077-0383/13/2/607

Internet

https://www.mdpi.com/2077-0383/13/2/607

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