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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

18-75 Years
All
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?

Yes

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

No

Exclusion Criteria

- Refusal to participate in research protocols

- Refusal to participate expressed following receipt of information letter.

Locations

Location

Status