Search for Phenotype-modifying Genes in Patients with Intellectual Disabilities.
Sponsored by University Hospital, Bordeaux
About this trial
Last updated 7 months ago
Study ID
CHUBX 2024 75
Status
Not yet recruiting
Type
Observational
Placebo
No
Accepting
All
All
Trial Timing
Started 6 months ago
What is this trial about?
Each form of intellectual disability under study is a rare disease in its own right, and
it is therefore difficult to study the variability of its expression. It therefore
appears necessary to study large series of patients with intellectual disabilities. The
objective is to identify variants in phenotype-modifying genes in patients with
intellectual disability.
What are the participation requirements?
Inclusion Criteria
- Patients with Intellectual Disability or related but not affected by them
- Major or minor with autorisation of legal representative
- Exome sequencing in Bordeaux University Hospital between 2018 and 2024
Exclusion Criteria
- Refusal to participate in research protocols
- Refusal to participate expressed following receipt of information letter.