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New Strategies of Genetic Study of Patients With Oculocutaneous Albinism — GENALB  

Mutation Clinical Trial

Official title:
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism

Clinical Trial Summary

The oculocutaneous albinism is an autosomal recessive condition associated with mutations in 4 genes. In 20% of patients no mutation is identified. The optimization of genetic analysis methods and the search for new genes involved will help improve the diagnosis in these patients.

Clinical Trial Description

The oculocutaneous albinism is an autosomal recessive condition associated with mutations in 4 genes. In 20% of patients no mutation is identified. The optimization of genetic analysis methods and the search for new genes involved will help improve the diagnosis in these patients.

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Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04068961
Study type Observational
Source University Hospital, Bordeaux
Contact
Status Completed
Phase
Start date September 15, 2010
Completion date October 31, 2010
View Details
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