Genetic Markers and Biomarkers in Patients With Intellectual Disabilities of Genetic Origin

Recruiting now · Not applicable

Conditions studied: Down Syndrome, Intellectual Disability

In brief

Analyze genetic and biological markers in patients with Intellectual Deficiencies (ID) of genetic origin in order to better understand the mechanisms of modified genes, cellular mechanisms, pathways involved in different disorders , complications and pathologies associated with ID of genetic origin.

Key facts

Study ID

NCT05767203

Run by

Institut Jerome Lejeune

People needed

2000

Starts

2022-09-01

Expected to finish

2032-12-31

Last updated by the study team

2023-03-14

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patient diagnosed with an intellectual disability of genetic origin
• Patient of all ages coming for consultation at the Institut Jérôme Lejeune
• Patient whose parents or legal representative have received and understood the information document and signed the informed consent for a sample for the research project.
• Patient affiliated to a social security scheme

You may not qualify if…

• Parents unable to find out about the constraints related to the study
• Refusal of informed patient participation
• Pregnant, parturient and nursing mothers
• Persons deprived of their liberty by judicial or administrative decision

Where it is running

• Institut Jérôme Lejeune — Paris, France (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.