Your browser doesn't support javascript.
loading
Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.
Bertoli-Avella, Aida M; Giroud-Benitez, Jose L; Bonifati, Vincenzo; Alvarez-Gonzalez, Eduardo; Heredero-Baute, Luis; van Duijn, Cornelia M; Heutink, Peter.
Afiliação
  • Bertoli-Avella AM; Department of Epidemiology and Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands. a.bertoliavella@erasmusmc.nl
Mov Disord ; 18(11): 1240-9, 2003 Nov.
Article em En | MEDLINE | ID: mdl-14639663
The identification of disease genes using family-based approaches has provided important insights into the pathogenesis of Parkinson's disease (PD) demonstrating the importance of genetic studies on monogenic forms of the disease. We studied a large Cuban family with typical, late-onset PD and probable autosomal dominant inheritance. Mean age at onset was 61.2 years (+/- 12.53, 45-76). Other phenotypes such as essential tremor and atypical parkinsonism were observed in this family. We carried out a genome-wide scan and linkage analyses. The genetic data were analyzed using a conservative model in which only patients with clinically definite or likely PD were considered affected, other phenotypes were regarded as "unknown." Multipoint analyses yielded a maximum LOD of 2.26 between markers D19S221 and D19S840. Haplotype analysis showed a region on chromosome 19 shared by six of seven PD patients. The essential tremor phenotype and the atypical parkinsonism do not segregate with this haplotype, suggesting a different etiology. Our findings suggest the presence of a novel locus for PD on chromosome 19p13.3-q12. We propose that an oligogenic model with moderate contribution of two or three genes rather than a "pure" monogenic model might explain better the wide range in age at onset, the reduced penetrance and the phenotypical variability observed in PD families.
Assuntos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Cromossomos Humanos Par 19 / Ligação Genética Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Cuba Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Cromossomos Humanos Par 19 / Ligação Genética Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Cuba Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos