Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease

Aniko Folhoffer, Peter Ferenci, Timea Csak, Andrea Horvath, Dalma Hegedus, Gabor Firneisz, Janos Osztovits, Janos Pal Kosa, Claudia Willheim-Polli, Laszlo Szonyi, Margit Abonyi, Peter Laszlo Lakatos, Ferenc Szalay

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Abstract

BACKGROUND/AIMS: Diagnosis of Wilson's disease may be difficult in patients presenting with liver disease and in asymptomatic siblings. The aim of the present study was to assess the impact of genetic testing for diagnosis of the disease in a large cohort (n=109) from Hungary. PATIENTS/METHODS: One hundred and nine patients with Wilson's disease were studied (65 men and 44 women; mean age at onset of symptoms: 20±9 years). Diagnosis of the disease was based on typical clinical and laboratory features (all had a Wilson's disease score of ≥4). H1069Q was assessed by the semi-nested polymerase chain reaction-based restriction fragment length polymorphism assay. H1069Q heterozygotes and H1069Q negative samples were then screened for mutations (on exons 6 to 20) by denaturating high-performance liquid chromatography and than sequenced on a genetic analyser. RESULTS: Twenty-three different mutations were found. H1069Q was the most frequent mutation in Hungary, detected in 77 patients (71%). Fourteen further known mutations were found by sequencing. We identified eight new mis-sense mutations not described before: N676I, S693Y, Y715H, M769L, W939C, P1273S, G1281D and G1341V. In 36/109 patients (33%) the diagnosis of Wilson's disease was established by adding mutational analysis. The Kayser-Fleischer ring was more frequent in H1069Q homozygous patients and their mean age at the time of diagnosis was higher than in patients heterozygous or negative for H1069Q. CONCLUSION: Eight novel mutations in addition to the 15 that are already known were found in Hungarian patients with Wilson's disease. Our results underline the importance and usefulness of genetic testing for patients presenting with liver disease and for family screening.

Original languageEnglish
Pages (from-to)105-111
Number of pages7
JournalEuropean Journal of Gastroenterology and Hepatology
Volume19
Issue number2
DOIs
Publication statusPublished - febr. 1 2007

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ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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