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Clinical Trial Summary

The aim of this study is to identify families with hereditary chronic tubulointerstitial renal diseases , characterize the phenotype and screen for mutations in known genesis (UMOD, REN, TCF2, NPHP1). Genome wide analysis will be performed in families without mutations identified.


Clinical Trial Description

- Inclusion of affected subjects with familial history of chronic renal failure, early gout ,renal cysts in several hospital in France

- Characterization of the phenotype; dosage of the urinary uromodulin in all subjects

- Collect DNA samples

- Screen for UMO mutations first

- Then for REN or TCF2 depending on the phenotype

- Validate the use of the dosage of urinary uromodulin for the diagnosis of UMOD associated disease.

- Identify new genes responsible for hereditary HTIN (Hereditary Tubulointerstitial Nephritis). ;


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


NCT number NCT01312727
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact
Status Completed
Phase N/A
Start date November 2010
Completion date July 2016

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