Type 2 Mayer-Rokitansky-Küster-Hauser syndrome (https://homosaurus.org/v3/homoit0002882)
| Type 2 Mayer-Rokitansky-Küster-Hauser syndrome |
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- People with Type 2 Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome have both the differences associated with MRKH syndrome and additional differences in other parts of their body, such as their fallopian tubes, kidneys, spine, or heart. A specific example of Type 2 MRKH known as Müllerian agenesis, Renal agenesis, Cervicothoracic Somite (MURCS) association, occurs when someone’s kidneys do not develop typically. They may have scoliosis or fused vertebrae in addition to the usual features of MRKH.
- Developed during an extended collaboration with interACT: Advocates for Intersex Youth, 2022-2023.
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Type 2 Mayer-Rokitansky-Küster-Hauser syndrome
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