Viewing Study NCT06475651

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Ignite Creation Date: 2025-12-24 @ 11:54 PM
Ignite Modification Date: 2026-02-23 @ 8:08 PM
Study NCT ID: NCT06475651
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-26
First Post: 2024-06-20
Is Gene Therapy: True
Has Adverse Events: False
Brief Title: Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset
Sponsor: Assistance Publique - Hôpitaux de Paris
Organization:
Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Rare Fetal Genetic Diseases View
None Congenital Malformation View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Congenital malformation View
None DNA methylation abnormalities View
None Episignature View
None CHD7 gene View
None KMT2D gene View
None HYLS1 gene View
None TCTN3 gene View
None FLVCR2 gene View
None CHARGE syndrome View
None KABUKI syndrome View