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Molecular Genetic Study of Mayer-Rokitansky-Kuster-Hauser Syndrome

Recruitingn/aAges any - anyAllImagine Institute
NCT02967822 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

In order to understand the molecular mechanisms leading to Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH), the research team has to identify molecular bases of this anomaly. Toward this goal, the research team would like to include in the study patients with MRKH syndrome, as well as their healthy relatives, in order to perform genetic analyses, especially whole exome sequencing. This study has been set up in order to collect biological samples from patients with MRKH and their relatives.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patient with MRKH syndrome OR healthy relative of patient included * Having signed the Informed consent form (or parents in case of patient under 18 years) Exclusion Criteria: * Refusal to participate in genetic analyses * Participation in a therapeutical clinical study in the 30 days prior to inclusion in the present study.
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What it tests

  • Biological samples for patients
  • Biological samples for healthy relatives
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Where

2 sites
Necker - Enfants malades hospital
Paris, France
Institut Mutualiste Montsouris
Paris, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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