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Article

[The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics].

Journal de gynecologie, obstetrique et biologie de la reproduction - 1 Oct 2008

Morcel K, Guerrier D, Watrin T, Pellerin I, Levêque J

Abstract excerpt

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (two-third) of the vagina. It may be isolated (type I) or associated with other malformations (type II or MURCS association). These latter involve the upper urinary tract, the skeleton and, to a lesser extent, the otologic sphere or the heart. The incidence of MRKH syndrome has been estimated...

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Identifiers

PMID: 18723299
DOI: 10.1016/j.jgyn.2008.07.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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