Literature DB >> 29563951

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.

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


  13 in total

1.  The mitochondrial genome in Wolfram syndrome.

Authors:  T G Barrett; M Scott-Brown; A Seller; A Bednarz; K Poulton; J Poulton
Journal:  J Med Genet       Date:  2000-06       Impact factor: 6.318

2.  Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified.

Authors:  Lars Hansen; Hans Eiberg; Timothy Barrett; Toke Bek; Per Kjaersgaard; Lisbeth Tranebjaerg; Thomas Rosenberg
Journal:  Eur J Hum Genet       Date:  2005-12       Impact factor: 4.246

3.  Ophthalmologic correlates of disease severity in children and adolescents with Wolfram syndrome.

Authors:  James Hoekel; Smith Ann Chisholm; Amal Al-Lozi; Tamara Hershey; Lawrence Tychsen
Journal:  J AAPOS       Date:  2014-10-21       Impact factor: 1.220

Review 4.  Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Authors:  Patrick Yu-Wai-Man; Philip G Griffiths; Patrick F Chinnery
Journal:  Prog Retin Eye Res       Date:  2010-11-26       Impact factor: 21.198

Review 5.  Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered?

Authors:  Timothy Geoffrey Barrett
Journal:  Pediatr Diabetes       Date:  2007-10       Impact factor: 4.866

6.  Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.

Authors:  A Cano; C Rouzier; S Monnot; B Chabrol; J Conrath; P Lecomte; B Delobel; P Boileau; R Valero; V Procaccio; V Paquis-Flucklinger; B Vialettes
Journal:  Am J Med Genet A       Date:  2007-07-15       Impact factor: 2.802

Review 7.  Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.

Authors:  Kim Cryns; Theru A Sivakumaran; Jody M W Van den Ouweland; Ronald J E Pennings; Cor W R J Cremers; Kris Flothmann; Terry-Lynn Young; Richard J H Smith; Marci M Lesperance; Guy Van Camp
Journal:  Hum Mutat       Date:  2003-10       Impact factor: 4.878

8.  Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype.

Authors:  Julia Rohayem; Christian Ehlers; Bärbel Wiedemann; Reinhard Holl; Konrad Oexle; Olga Kordonouri; Giuseppina Salzano; Thomas Meissner; Walter Burger; Edith Schober; Angela Huebner; Min Ae Lee-Kirsch
Journal:  Diabetes Care       Date:  2011-05-20       Impact factor: 19.112

9.  Phenotypic characteristics of early Wolfram syndrome.

Authors:  Bess A Marshall; M Alan Permutt; Alexander R Paciorkowski; James Hoekel; Roanne Karzon; Jon Wasson; Amy Viehover; Neil H White; Joshua S Shimony; Linda Manwaring; Paul Austin; Timothy E Hullar; Tamara Hershey
Journal:  Orphanet J Rare Dis       Date:  2013-04-27       Impact factor: 4.123

10.  Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.

Authors:  Giuseppe d'Annunzio; Nicola Minuto; Elena D'Amato; Teresa de Toni; Fortunato Lombardo; Lorenzo Pasquali; Renata Lorini
Journal:  Diabetes Care       Date:  2008-06-19       Impact factor: 19.112

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  2 in total

1.  Wolfram syndrome with a rare genetic mutation - Case report.

Authors:  Divya U Caculo; Sowmya Raveendra Murthy; Ankita A Patil; Sneha R Peswani
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

2.  Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Authors:  Jinying Li; Hongen Xu; Jianfeng Sun; Yongan Tian; Danhua Liu; Yaping Qin; Huanfei Liu; Ruijun Li; Lingling Neng; Xiaohua Deng; Binbin Xue; Changyun Yu; Wenxue Tang
Journal:  Biomed Res Int       Date:  2021-03-04       Impact factor: 3.411

  2 in total

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