Mayer-Rokitansky-Küster-Hauser syndrome (https://fr.homosaurus.org/v3/homoit0002865)




Identifiant
homoit0002865
Étiquette privilégiée
Mayer-Rokitansky-Küster-Hauser syndrome
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Étiquette alternative
MRKH syndrome
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Müllerian agenesis
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Müllerian duct anomalies
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Müllerian duct variations
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Description
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome occurs when a person's Müllerian ducts, which typically become the uterus and upper portion of the vagina during fetal development, do not develop in the typical way. People with MRKH have XX chromosomes and are usually born with a vulva and either a vagina that is shorter than typical or no vagina. They usually do not have a cervix and may have a partial uterus (uterine remnant) or no uterus. They often do not mensturate but may experience cyclic pain if they have a uterine remnant with endometrial lining, and they can develop menstruation-related conditions like endometriosis.
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Contributeurs
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
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Publié (Créé)
2023-06-28 18:15:40 UTC
Modifié
2025-02-23 07:12:58 UTC
Plus large
Intersex variations [homoit0000669]
Plus précis
Type 1 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002880]
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002882]

Affichage de la hiérarchie

Intersex variations
Mayer-Rokitansky-Küster-Hauser syndrome
Type 1 Mayer-Rokitansky-Küster-Hauser syndrome
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome


Autres formats (y compris les identifiants de langue): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Formats hérités (sans identifiants de langue) N-Triples, JSON-LD, TTL

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