Status:
COMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome.
Lead Sponsor:
University Hospital, Bordeaux
Conditions:
Goldenhar Syndrome
Oculoauriculovertebral Dysplasia
Eligibility:
All Genders
Brief Summary
The aim of this study is to identify of the first gene involved in the Goldenhar syndrome in a cohort of 120 affected patients.
Detailed Description
Goldenhar syndrome belongs to the heterogeneous spectrum of oculoauriculovertebral dysplasia. Several chromosomal abnormalities have been described associated with this spectrum, and furthermore mutat...
Eligibility Criteria
Inclusion
- Spectrum of oculoauriculovertebral dysplasia minimal features include unilateral microtia and hemifacial microsomia
Exclusion
- Absence of minimal spectrum of oculoauriculovertebral dysplasia features, molecular anomaly identified, other diagnosis
Key Trial Info
Start Date :
September 29 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 8 2014
Estimated Enrollment :
248 Patients enrolled
Trial Details
Trial ID
NCT04056858
Start Date
September 29 2012
End Date
January 8 2014
Last Update
August 14 2019
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.