Homosaurus Vocabulary Site

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

homoit0002865

Mayer-Rokitansky-Küster-Hauser syndrome

ইংরেজি

MRKH syndrome	ইংরেজি
Müllerian agenesis	ইংরেজি
Müllerian duct anomalies	ইংরেজি
Müllerian duct variations	ইংরেজি

বিবরণ

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.

ইংরেজি

অবদানকারী

Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.

ইংরেজি

ইস্যু করা হয়েছে (তৈরি করা হয়েছে)

2023-06-28 18:15:40 UTC

পরিবর্তিত

2025-02-23 07:12:58 UTC

বিস্তৃত পরিভাষা

Intersex variations [homoit0000669]

সংকীর্ণ পরিভাষা

Type 1 Mayer-Rokitansky-Küster-Hauser syndrome [homoit0002880]