Inter-regional Project of the Great Western Exploration Approach for Exome Molecular Causes Severe Intellectual Disability Isolated or Syndromic

NCT ID: NCT02136849

Last Updated: 2018-12-12

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 228 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2014-09-30
• Study Completion Date: 2016-01-31

Brief Summary

Intellectual disability (ID) moderate or severe affects about one child in 250, with 3000 to 4000 new cases each year. Chromosomal or molecular pathology causes are not identified in half of the cases by current techniques. Studies show that de novo mutations are common in many different genes. The "exome" approach by high-throughput sequencing (NGS) has emerged as the technique of choice for identifying and comparing the exome of the child to the parent. We wish to evaluate this approach and its contribution in the diagnostic management of 50 patients with DI seen in genetics in 6 CHU Great West. Genomics platform IBISA / Biogenouest will provide technological and bioinformatics support this project.

Conditions

Severe Intellectual Disability

Keywords

severe intellectual disability, genetic, de novo exome

Study Design

• Observational Model Type: FAMILY_BASED
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Patients with severe intellectual disability (IQ <35 ) or moderate (IQ <50) isolated or syndromic presentation but undiagnosed . The diagnosis is established during genetic counseling of a 6 CHU interregion
• Lack of family history ( parents). We are interested in this project to patients who do not have family history in order to increase the probability of identifying a de novo mutation . We do not however exclude the hypothesis for some patients a mechanism recessive autosomal or X-linked .
• Recruitment in 6 CHU HUGO . Patients are required to have been seen in genetics in a 6 CHU interregion . Molecular analyzes of the Fragile X syndrome and the CGH technique must be negative.
• Indication sequencing exomique adopted by the Scientific Committee. The Scientific Committee HUGODIMS project role to select patients whose DNA will be studied in order to optimize the chances of success for sequencing . This selection must take into account clinical parameters , but also genetic parameters ( potential inbreeding ) . The files will be selected by videoconferencing at the end of the monthly meeting of CLAD . The methodologist of the study will be invited to videoconferencing.
• specific consent obtained for the study.

Exclusion Criteria

• Parents patient with moderate or severe intellectual disability disagree with the preferred hypothesis of de novo mutation or recessive transmission mechanism.
• Form with known syndromic diagnosis can be targeted molecular studies (clinical signs).
• Cause molecular DI identified by targeted molecular analysis or CGH.
• Explicit refusal to participate in the study of the patient, parents, or one of the two parents.
• Any other indication that intellectual disability.
• The parents of the patient or the patient may be removed.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Nantes Genomics platform

UNKNOWN

Sponsor Role: collaborator

Nantes University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stéphane Bézieau, Pr

Role: PRINCIPAL_INVESTIGATOR

Nantes University Hospital

Locations

Angers University Hospital

Angers, , France

Brest University Hospital

Brest, , France

Poitiers University Hospital

Poitiers, , France

Rennes University Hospital

Rennes, , France

Tours University Hospital

Tours, , France

Countries

France

Other Identifiers

RC14_0107

Identifier Type: -

Identifier Source: org_study_id