01
Rare congenital condition
MRKH syndrome & neovagina formation
MRKH (Mayer–Rokitansky–Küster–Hauser) syndrome affects development of the uterus and upper vagina. Care is private, unhurried and centred on the person's goals, anatomy and readiness for treatment.
What the care plan considers
- Careful review of MRI or ultrasound findings and any associated kidney or skeletal differences
- Clear discussion of non-surgical vaginal dilation, which is often considered first when appropriate
- Individualised neovagina planning when surgery is preferred or clinically suitable
- Long-term support for healing, vaginal function and emotional wellbeing
1
Confirm anatomy
2
Discuss every option
3
Shared treatment decision
4
Structured follow-up