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




Identifierare
homoit0002865
Föredragen benämning
Mayer-Rokitansky-Küster-Hauser syndrome
English
Variant
MRKH syndrome
English
Müllerian agenesis
English
Müllerian duct anomalies
English
Müllerian duct variations
English
Beskrivning
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
Bidragsgivare
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
Bredare
Intersex variations [homoit0000669]
Smalare
Type 1 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002880]
Type 2 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002882]

Hierarkisk vy

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


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Äldre format (utan språkidentifierare) N-Triples, JSON-LD, TTL

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