MRKH syndrome
Conditions
Interventions
96 patients with MRKH will be included. The controlgroup exists of 96 healthy women, already sampled. No interventions. Blood samples will be analyzed for Y-chromosome-specific real-time quantitative
Sponsors
VU university medical centre
Eligibility
Inclusion criteria
Inclusion criteria: - Diagnosed with MRKH syndrome - Age ≥ 18 years
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the difference in occurrence of microchimerism (with an extra male cell line) in MRKH patients vs. controls. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome is the presence of chimerism in non-hematopoietic tissue (buccal cells) in MRKH patients. | — |
Contacts
Public ContactHenrike Peters
VUmc, afdeling reproductive medicine. PK 5x -194.
Outcome results
None listed