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Clinical Trial Summary

This study is based on the study of the natural history of a rare disorder: the Bardet-Biedl syndrome (BBS) (which is associated with retinitis pigmentosa, polydactyly, cognitive impairment, obesity, and kidney failure). The clinical, biological, and radiological features of adult patients are studied. In parallel, a molecular study is performed on the known genes to date (8 genes from BBS1 to BBS8) and to identify new genes involved. The parts of the study are combined in a phenotype-genotype correlation study.


Clinical Trial Description

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Study Design

N/A


Related Conditions & MeSH terms


NCT number NCT00213811
Study type Observational
Source University Hospital, Strasbourg, France
Contact
Status Completed
Phase N/A
Start date June 2003

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