Ignite Creation Date:
2024-05-06 @ 7:48 PM
Last Modification Date:
2024-10-26 @ 3:14 PM
Study NCT ID:
NCT06147414
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-02-28
First Post:
2023-09-18
Brief Title:
Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders
Sponsor:
Assistance Publique - Hôpitaux de Paris
Organization:
Assistance Publique - Hôpitaux de Paris
Conditions & Keywords Data
Conditions:
| Name |
|---|
| 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 |
| MODY2 Diabetes |
| X-Linked Hydrocephalus |
| Autosomal Recessive Polycystic Kidney Disease |