Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for OPA1/OPA3/LHON |
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Authors: | Alberto Galvez-Ruiz Alicia Galindo-Ferreiro Patrik Schatz |
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Affiliation: | 1. King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia;2. Department of Ophthalmology, Clinical Sciences, Scane County University Hospital, University of Lund, Lund, Sweden |
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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. |
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Keywords: | Central diabetes insipidus diabetes mellitus hereditary optic neuropathies neurosensory deafness optic atrophy Wolfram syndrome |
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