Literature DB >> 25327413

Families with Wilson's disease in subsequent generations: clinical and genetic analysis.

Karolina Dzieżyc1, Tomasz Litwin, Grzegorz Chabik, Karolina Gramza, Anna Członkowska.   

Abstract

INTRODUCTION: Wilson's disease is an inherited autosomal recessive disorder of copper metabolism. The prevalence of Wilson's disease in most populations is approximately 1 in 30,000. The risk for offspring is 0.5%. The aim of this study was to establish the frequency of disease among offspring of a cohort of Wilson's disease patients.
MATERIALS AND METHODS: In February 2014, our registry included 760 cases of diagnosed Wilson's disease. We selected families in which Wilson's disease was diagnosed in the proband's offspring.
RESULTS: Between 1957 and 2014, 1,050 relatives of affected members were screened. Wilson's disease in subsequent generations was observed in nine non-consanguineous families, with 12 affected offspring from nine probands.
CONCLUSION: We detected a higher (4.08%) than expected (0.5%) frequency of Wilson's disease among proband offspring, which is in accordance with a recent genetic study in the United Kingdom that suggested a higher WD prevalence in the European population.
© 2014 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  Wilson's disease; consecutive generations; family screening

Mesh:

Substances:

Year:  2014        PMID: 25327413     DOI: 10.1002/mds.26057

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  7 in total

1.  Difficulties in diagnosis and treatment of Wilson disease-a case series of five patients.

Authors:  Anna Członkowska; Karolina Dzieżyc-Jaworska; Bożena Kłysz; Rędzia-Ogrodnik Barbara; Tomasz Litwin
Journal:  Ann Transl Med       Date:  2019-04

Review 2.  Wilson disease.

Authors:  Anna Członkowska; Tomasz Litwin; Petr Dusek; Peter Ferenci; Svetlana Lutsenko; Valentina Medici; Janusz K Rybakowski; Karl Heinz Weiss; Michael L Schilsky
Journal:  Nat Rev Dis Primers       Date:  2018-09-06       Impact factor: 52.329

3.  Molecular genetic diagnosis of Wilson disease by ARMS-PCR in a Pakistani family.

Authors:  Haq Nawaz Khan; Muhammad Wasim; Hina Ayesha; Fazli Rabbi Awan
Journal:  Mol Biol Rep       Date:  2018-11-13       Impact factor: 2.316

Review 4.  The genetics of Wilson disease.

Authors:  Irene J Chang; Si Houn Hahn
Journal:  Handb Clin Neurol       Date:  2017

5.  Rapid and reliable diagnosis of Wilson disease using X-ray fluorescence.

Authors:  Slávka Kaščáková; Cameron M Kewish; Stéphan Rouzière; Françoise Schmitt; Rodolphe Sobesky; Joël Poupon; Christophe Sandt; Bruno Francou; Andrea Somogyi; Didier Samuel; Emmanuel Jacquemin; Anne Dubart-Kupperschmitt; Tuan Huy Nguyen; Dominique Bazin; Jean-Charles Duclos-Vallée; Catherine Guettier; François Le Naour
Journal:  J Pathol Clin Res       Date:  2016-06-06

6.  Characteristics of a newly diagnosed Polish cohort of patients with neurological manifestations of Wilson disease evaluated with the Unified Wilson's Disease Rating Scale.

Authors:  Anna Członkowska; Tomasz Litwin; Karolina Dzieżyc; Michal Karliński; Johan Bring; Carl Bjartmar
Journal:  BMC Neurol       Date:  2018-04-05       Impact factor: 2.474

7.  Characterization of Fibrinogen as a Key Modulator in Patients with Wilson's Diseases with Functional Proteomic Tools.

Authors:  Pei-Wen Wang; Tung-Yi Lin; Yu-Chiang Hung; Wen-Neng Chang; Pei-Ming Yang; Mu-Hong Chen; Chau-Ting Yeh; Tai-Long Pan
Journal:  Int J Mol Sci       Date:  2019-09-12       Impact factor: 5.923

  7 in total

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