Clinical, Molecular and Physiopathological Study of Cohen Syndrome and Cohen-like Syndromes
NCT01907555 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2018-01-31
Summary
This project will make it possible to better understand the natural history of Cohen Syndrom and the phenotypes associated with mutations in the VPS13B gene, to improve the therapeutic management of patients. It will also provide a better description of Cohen-like syndrome for genetic counselling for the families concerned.
Conditions
- Cohen Syndrome
Sponsors & Collaborators
-
Centre Hospitalier Universitaire Dijon
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-07-24
- Primary Completion
- 2016-09-13
- Completion
- 2016-09-13
Countries
- France
Study Locations
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