U.S., March 21 -- ClinicalTrials.gov registry received information related to the study (NCT07485413) titled 'Looking for VUS to Confirm Dominant Wolfram-like Syndrome Instead of Recessive Wolfram Syndrome' on March 08.
Brief Summary: Looking for the pthogenicity of mutations of WFS1 gene for patients with mutation of the two alleles but a dominant phenotype
Study Start Date: March 08
Study Type: OBSERVATIONAL
Condition:
Optical Coherence Tomography (OCT) of the Retina
Mutation
Recruitment Status: ACTIVE_NOT_RECRUITING
Sponsor: Hopital Necker-Enfants Malades
Information provided by (Responsible Party): Christophe Orssaud, Hopital Necker-Enfants Malades
Disclaimer: Curated by HT Syndication....