| Literature DB >> 29563951 |
Alberto Galvez-Ruiz1, Alicia Galindo-Ferreiro1, Patrik Schatz1,2.
Abstract
In this study, the authors present a sample of 71 patients with hereditary optic neuropathy and negative genetic test results for OPA1/OPA3/LHON. All of these patients later underwent genetic testing to rule out WFS. As a result, 53 patients (74.7%) were negative and 18 patients (25.3%) were positive for some type of mutation or variation in the WFS gene. The authors believe that this study is interesting because it shows that a sizeable percentage (25.3%) of patients with hereditary optic 25 neuropathy and negative genetic test results for OPA1/OPA3/LHON had WFS mutations or variants.Entities:
Keywords: Central diabetes insipidus; Wolfram syndrome; diabetes mellitus; hereditary optic neuropathies; neurosensory deafness; optic atrophy
Year: 2017 PMID: 29563951 PMCID: PMC5858862 DOI: 10.1080/01658107.2017.1344252
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107