G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
Identifieur interne : 000E44 ( PubMed/Checkpoint ); précédent : 000E43; suivant : 000E45G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
Auteurs : Suzanne Lesage ; Pablo Ibanez ; Ebba Lohmann ; Pierre Pollak ; François Tison ; Myriem Tazir ; Anne-Louise Leutenegger ; Joao Guimaraes ; Anne-Marie Bonnet ; Yves Agid [France] ; Alexandra Dürr ; Alexis BriceSource :
- Annals of neurology [ 0364-5134 ] ; 2005.
English descriptors
- KwdEn :
- Adult, Africa, Northern (epidemiology), Africa, Northern (ethnology), Aged, Aged, 80 and over, DNA Mutational Analysis (methods), Family Health, Female, France (epidemiology), France (ethnology), Gene Frequency, Genetic Predisposition to Disease, Genotype, Glycine (genetics), Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Mental Status Schedule (statistics & numerical data), Middle Aged, Mutation, Parkinson Disease (genetics), Protein-Serine-Threonine Kinases (genetics), Serine (genetics).
- MESH :
- chemical , genetics : Glycine, Protein-Serine-Threonine Kinases, Serine.
- epidemiology : Africa, Northern, France.
- ethnology : Africa, Northern, France.
- genetics : Parkinson Disease.
- methods : DNA Mutational Analysis.
- statistics & numerical data : Mental Status Schedule.
- Adult, Aged, Aged, 80 and over, Family Health, Female, Gene Frequency, Genetic Predisposition to Disease, Genotype, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Middle Aged, Mutation.
Abstract
Mutations in LRRK2 were recently identified in autosomal dominant Parkinson's disease (PD), including the G2019S mutation. To evaluate its frequency, we analyzed 198 probands with autosomal dominant PD, mostly from France and North Africa. Surprisingly, the frequency in North African families (7/17, 41%) was greater than those from Europe (5/174, 2.9%). The clinical features in 21 patients, including 1 with a homozygous mutation, were those of typical PD, with lower Mini-Mental State Examination scores. There were also 15 unaffected mutation carriers, aged 32 to 74 years. LRRK2 mutations appear to be a common cause of autosomal dominant PD, particularly in North Africa.
DOI: 10.1002/ana.20636
PubMed: 16240353
Affiliations:
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Links to Exploration step
pubmed:16240353Le document en format XML
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<front><div type="abstract" xml:lang="en">Mutations in LRRK2 were recently identified in autosomal dominant Parkinson's disease (PD), including the G2019S mutation. To evaluate its frequency, we analyzed 198 probands with autosomal dominant PD, mostly from France and North Africa. Surprisingly, the frequency in North African families (7/17, 41%) was greater than those from Europe (5/174, 2.9%). The clinical features in 21 patients, including 1 with a homozygous mutation, were those of typical PD, with lower Mini-Mental State Examination scores. There were also 15 unaffected mutation carriers, aged 32 to 74 years. LRRK2 mutations appear to be a common cause of autosomal dominant PD, particularly in North Africa.</div>
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<Abstract><AbstractText>Mutations in LRRK2 were recently identified in autosomal dominant Parkinson's disease (PD), including the G2019S mutation. To evaluate its frequency, we analyzed 198 probands with autosomal dominant PD, mostly from France and North Africa. Surprisingly, the frequency in North African families (7/17, 41%) was greater than those from Europe (5/174, 2.9%). The clinical features in 21 patients, including 1 with a homozygous mutation, were those of typical PD, with lower Mini-Mental State Examination scores. There were also 15 unaffected mutation carriers, aged 32 to 74 years. LRRK2 mutations appear to be a common cause of autosomal dominant PD, particularly in North Africa.</AbstractText>
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