Literature DB >> 21564155

Wolfram syndrome in the Polish population: novel mutations and genotype-phenotype correlation.

A Zmyslowska1, M Borowiec, K Antosik, M Szalecki, A Stefanski, B Iwaniszewska, M Jedrzejczyk, I Pietrzak, W Mlynarski.   

Abstract

OBJECTIVE: Wolfram syndrome is a rare form of diabetes mellitus associated with optic atrophy and disorders of different organs (e.g. diabetes insipidus, hearing loss, ataxia, anaemia and many others). This syndrome is caused by recessive mutations in the wolframin gene (WFS1) localized on chromosome 4p16·1. The aim of this study was to identify the causative mutations in WFS1 in a group of Polish patients with suspected Wolfram syndrome. PATIENTS AND MEASUREMENTS: Nine patients with clinical symptoms consistent with Wolfram syndrome (at least diabetes mellitus and optic atrophy) and 22 first-degree relatives were examined. The molecular analysis was carried out by direct sequencing of the exons, the exon-intron junctions, and the 5' and 3' untranslated regions of WFS1.
RESULTS: Nine different mutations in WFS1 (five of them novel) were identified in the nine patients. Six patients were homozygous for the following mutations: V412fs, S443R, W539X, V659fs. They developed diabetes at a mean age of 5·2 years. Three patients were compound-heterozygous for the following mutations: S167fs, Q392X, Y513fs, W648X, V779G. They developed diabetes at a mean age of 6·5 years.
CONCLUSIONS: Mean age of diagnosis of diabetes among the Polish patients was typical for Wolfram syndrome; however, compound-heterozygous patients were slightly older at diabetes onset.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21564155     DOI: 10.1111/j.1365-2265.2011.04102.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  10 in total

1.  Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Authors:  Maryam Sobhani; Mohammad Amin Tabatabaiefar; Soudeh Ghafouri-Fard; Asadollah Rajab; Sarah Mozafarpour; Samaneh Nasrniya; Abdol-Mohammad Kajbafzadeh; Mohammad Reza Noori-Daloii
Journal:  Endocrine       Date:  2019-07-16       Impact factor: 3.633

2.  Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.

Authors:  Ziyu Ren; Jixiu Yi; Min Zhong; Yunting Wang; Qicong Liu; Xuan Wang; Dongfang Liu; Wei Ren
Journal:  BMC Endocr Disord       Date:  2021-08-17       Impact factor: 2.763

3.  Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndrome.

Authors:  Agnieszka Zmyslowska; Bogdan Malkowski; Wojciech Fendler; Maciej Borowiec; Karolina Antosik; Piotr Gnys; Dobromila Baranska; Wojciech Mlynarski
Journal:  PLoS One       Date:  2014-12-26       Impact factor: 3.240

4.  Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.

Authors:  Maryam Sobhani; Mohammad Amin Tabatabaiefar; Soudeh Ghafouri-Fard; Asadollah Rajab; Asal Hojjat; Abdol-Mohammad Kajbafzadeh; Mohammad Reza Noori-Daloii
Journal:  BMC Med Genet       Date:  2020-01-14       Impact factor: 2.103

5.  Serum microRNA as indicators of Wolfram syndrome's progression in neuroimaging studies.

Authors:  Maciej Borowiec; Wojciech Młynarski; Agnieszka Zmyslowska; Marcin Stanczak; Zuzanna Nowicka; Arleta Waszczykowska; Dobromila Baranska; Wojciech Fendler
Journal:  BMJ Open Diabetes Res Care       Date:  2020-11

Review 6.  Urinary Tract Involvement in Wolfram Syndrome: A Narrative Review.

Authors:  Alberto La Valle; Gianluca Piccolo; Mohamad Maghnie; Giuseppe d'Annunzio
Journal:  Int J Environ Res Public Health       Date:  2021-11-15       Impact factor: 3.390

7.  Multiomic analysis on human cell model of wolfram syndrome reveals changes in mitochondrial morphology and function.

Authors:  Wojciech Mlynarski; Wojciech Fendler; Agnieszka Zmyslowska; Miljan Kuljanin; Beata Malachowska; Marcin Stanczak; Dominika Michalek; Aneta Wlodarczyk; Dagmara Grot; Joanna Taha; Bartłomiej Pawlik; Magdalena Lebiedzińska-Arciszewska; Hanna Nieznanska; Mariusz R Wieckowski; Piotr Rieske; Joseph D Mancias; Maciej Borowiec
Journal:  Cell Commun Signal       Date:  2021-11-20       Impact factor: 5.712

8.  Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings.

Authors:  Xin Zhang; Yue Xie; Ke Xu; Haoyu Chang; Xiaohui Zhang; Yang Li
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-09-01       Impact factor: 4.925

9.  Glycemic variability in patients with Wolfram syndrome is lower than in type 1 diabetes.

Authors:  A Zmyslowska; W Fendler; A Szadkowska; M Borowiec; M Mysliwiec; A Baranowska-Jazwiecka; M Buraczewska; M Fulmanska-Anders; B Mianowska; I Pietrzak; D Rzeznik; W Mlynarski
Journal:  Acta Diabetol       Date:  2015-04-29       Impact factor: 4.280

10.  Retinal thickness as a marker of disease progression in longitudinal observation of patients with Wolfram syndrome.

Authors:  Agnieszka Zmyslowska; Wojciech Fendler; Arleta Waszczykowska; Anna Niwald; Maciej Borowiec; Piotr Jurowski; Wojciech Mlynarski
Journal:  Acta Diabetol       Date:  2017-08-30       Impact factor: 4.280

  10 in total

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