Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

Clinical trial NCT06147414 · RECRUITING

Trial details

NCT number: NCT06147414
Sponsor: Assistance Publique - Hôpitaux de Paris
Status: RECRUITING
Study type: OBSERVATIONAL

Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Including Sickle Cell Disease Cystic Fibrosis Fragile X Syndrome Proximal Spinal Muscular Atrophy Myotonic Dystrophy Muscular Dystrophy, Duchenne Muscular Dystrophy, Becker Neurofibromatosis-Noonan Syndrome Huntington Disease Hemophilia A Hemophilia B

Start date: 2024-10-23
Primary completion: 2027-05-01
Enrollment: 550

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