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Clinical Trial Summary

As principal objective, the study aims to:

1. Describe the spectrum and evaluate the frequency of angiodysplasia of the nevrax;

2. Establish the physiopathological basis of Fowler's syndrome;

3. Identify FLVCR2 partners and the signaling pathways involved;

4. Test new candidate genes: GPR124 and possible partners of FLVCR2.

As second objective, the study aims to:

- perform phenotype / genotype correlation if necessary;

- and propose a prenatal diagnosis in families with identified mutations.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03293134
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact
Status Completed
Phase N/A
Start date July 8, 2013
Completion date October 6, 2016