Department of Genomic Medicine for Rare Diseases and the Multidisciplinary Center for Prenatal Diagnosis of the Necker-Enfants malades Hospital

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset	Abnormalities, Multiple, CHARGE syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Kabuki syndrome, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, blindness (disorder), coloboma, eye disorder, hearing disorder, hearing loss disorder, hereditary disease, hydrolethalus syndrome 1, nervous system disorder, otorhinolaryngologic disease, vision disorder	Recruiting	Not stated	2026-03-27		NCT06475651

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