Síndrome de Mayer-Rokitansky-Küster-Hauser (https://es.homosaurus.org/v3/homoit0002865)




Identificador
homoit0002865
Etiqueta preferida
Mayer-Rokitansky-Küster-Hauser syndrome
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Etiqueta alternativa
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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Descripción
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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Colaboradores
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
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Emitido (creado)
2023-06-28 18:15:40 UTC
Modificado
2025-02-23 07:12:58 UTC
Más amplio
Variaciones intersex [homoit0000669]
Más específico
Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 1 [homoit0002880]
Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2 [homoit0002882]

Visualización de jerarquía

Variaciones intersex
Síndrome de Mayer-Rokitansky-Küster-Hauser
Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 1
Síndrome de Mayer-Rokitansky-Küster-Hauser tipo 2


Otros formatos (incluidos identificadores de idioma): N-Triples, JSON-LD, Extended JSON, TTL, XML, MARC XML


Formatos heredados (sin identificadores de idioma) N-Triples, JSON-LD, TTL

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