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




Identificador
homoit0002865
Etiqueta preferida
Mayer-Rokitansky-Küster-Hauser syndrome
English
Etiqueta alternativa
MRKH syndrome
English
Müllerian agenesis
English
Müllerian duct anomalies
English
Müllerian duct variations
English
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.
English
Colaboradores
Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
English
Issued (Created)
2023-06-28 18:15:40 UTC
Modified
2023-06-28 18:15:40 UTC
Más amplio
Intersex variations [homoit0000669]
Más específico
Type 1 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002880]
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002882]

Visualización de jerarquía

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


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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