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Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis — FAMILYVASC  

Vasculitis Clinical Trial

Official title:
Identification of Susceptibility Loci and Genes for Systemic Vasculitis Risk, by Analyzing Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis (FAMILYVASC Study)

Clinical Trial Summary

The FAMILYVASC study is a prospective observational study which will aim to identify susceptibility loci and genes for systemic vasculitis risk in patients with familial or pediatric forms of vasculitis. Genetic analysis based on whole exome sequencing will be carried out through salivary DNA.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04006535
Study type Observational
Source French Vasculitis Study Group
Contact Benjamin Terrier, MD, PhD
Phone +33 1 58 41 14 61
Email benjamin.terrier@aphp.fr
Status Recruiting
Phase
Start date June 1, 2019
Completion date June 1, 2029
View Details
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