Trials / Completed
CompletedNCT02862808
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 18 (actual)
- Sponsor
- Centre Hospitalier Universitaire de Besancon · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Evaluation of diagnostic whole exome sequencing in patients with syndromic or isolated severe intellectual disability without a molecular diagnostic, with suspected autosomal recessive inheritance, allowing accurate genetic counseling in this high risk of recurrence group of diseases
Conditions
Timeline
- Start date
- 2019-03-15
- Primary completion
- 2019-12-03
- Completion
- 2019-12-03
- First posted
- 2016-08-11
- Last updated
- 2020-07-22
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT02862808. Inclusion in this directory is not an endorsement.