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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.
Galvez-Ruiz, Alberto; Galindo-Ferreiro, Alicia; Schatz, Patrik.
Afiliação
  • Galvez-Ruiz A; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
  • Galindo-Ferreiro A; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
  • Schatz P; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Neuroophthalmology ; 42(2): 73-82, 2018 Apr.
Article em En | MEDLINE | ID: mdl-29563951
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article