NCT07008612View on ClinicalTrials.gov

MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder

RecruitingOBSERVATIONAL
Enrollment

50

Participants

Timeline

Start Date

February 4, 2025

Primary Completion Date

May 1, 2027

Study Completion Date

November 1, 2027

Conditions
MYT1L Syndrome
Interventions
DIAGNOSTIC_TEST

Patients with a genetic syndrome linked to the MYT1L gene

"* Neuropsychological assessment by the neuropsychologist (lasting 1h30)~* Speech and language assessment (including language and prosody) by the speech therapist, lasting 1h30"

DIAGNOSTIC_TEST

Patients with a neurodevelopmental disorder of genetic origin but not linked to MYT1L

Evaluation de la prosodie par l'orthophoniste (45 minutes)

Trial Locations (1)

76031

RECRUITING

University Hospital of Rouen, Rouen

All Listed Sponsors
lead

University Hospital, Rouen

OTHER