Literature DB >> 3876678

Epidemiologic study of hepatolenticular degeneration (Wilson's disease) in Sardinia (1902-1983).

A Giagheddu, L Demelia, G Puggioni, A M Nurchi, L Contu, G Pirari, A Deplano, M G Rachele.   

Abstract

From 1902 to 1983, 68 cases of hepatolenticular degeneration (HLD) were discovered in Sardinia, with a mean frequency, in reference to number of live births, of 27.7 and a sex ratio of 1.83. The prevalence of the disease was seen to be higher over the last few decades. With regard to the geographic distribution of the disease, 3 high-frequency areas were evident, in Barbagia, in Campidano, and in the area surrounding the city of Sassari. In 38.23% of cases, the clinical picture was of hepatoneurologic type; hepatic forms have become more frequent over the last decades. The first symptoms were observed at mean age of 15 years 8 months. The number of asymptomatic cases was fairly consistent (22.05%). The median survival rate in subjects who received inadequate therapy was 6 years 4 months. Only 3 patients of the 45 treated with adequate therapy died. The gene frequency, calculated by the application of Dahlberg's formula, was extremely high.

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Year:  1985        PMID: 3876678     DOI: 10.1111/j.1600-0404.1985.tb01546.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  16 in total

1.  Wilson's disease: A review of what we have learned.

Authors:  Kryssia Isabel Rodriguez-Castro; Francisco Javier Hevia-Urrutia; Giacomo Carlo Sturniolo
Journal:  World J Hepatol       Date:  2015-12-18

2.  Effects of long-term treatment in Wilson's disease with D-penicillamine and zinc sulphate.

Authors:  A Czlonkowska; J Gajda; M Rodo
Journal:  J Neurol       Date:  1996-03       Impact factor: 4.849

3.  Wilson's disease in Scotland.

Authors:  R H Park; P McCabe; G S Fell; R I Russell
Journal:  Gut       Date:  1991-12       Impact factor: 23.059

4.  Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.

Authors:  A Figus; R Lampis; M Devoto; M S Ristaldi; A Ideo; S de Virgilis; A M Nurchi; A Corrias; R Corda; M E Lai
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

Review 5.  Population screening and diagnostic strategies in screening family members of Wilson's disease patients.

Authors:  Huamei Li; Ran Tao; Lifang Liu; Shiqiang Shang
Journal:  Ann Transl Med       Date:  2019-04

6.  Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.

Authors:  L A Farrer; B Bonne-Tamir; M Frydman; A Magazanik; K K Kidd; A M Bowcock; L L Cavalli-Sforza
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

7.  An epidemiological study of Wilson's disease in the Republic of Ireland.

Authors:  M Reilly; L Daly; M Hutchinson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-03       Impact factor: 10.154

8.  The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population.

Authors:  Alessandro Gialluisi; Simona Incollu; Tommaso Pippucci; Maria Barbara Lepori; Antonietta Zappu; Georgios Loudianos; Giovanni Romeo
Journal:  Eur J Hum Genet       Date:  2013-03-13       Impact factor: 4.246

9.  Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.

Authors:  A M Bowcock; J Tomfohrde; J Weissenbach; B Bonne-Tamir; P St George-Hyslop; M Giagheddu; L L Cavalli-Sforza; L A Farrer
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

10.  Neurological and neuropsychiatric spectrum of Wilson's disease: a prospective study of 45 cases.

Authors:  W Oder; G Grimm; H Kollegger; P Ferenci; B Schneider; L Deecke
Journal:  J Neurol       Date:  1991-08       Impact factor: 4.849

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