Source:http://linkedlifedata.com/resource/pubmed/id/15324609
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2004-8-24
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pubmed:abstractText |
The past several years have been marked by significant progress in identifying genetic anomalies in stroke-prone probands. These advances have occurred in both highly penetrant single-gene disorders and in common stroke, which is influenced by risk/susceptibility genes. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) can be challenging to diagnose because of the wide range of notch 3 mutations that can cause disease, but a new immunohistochemical technique using a skin biopsy sample appears to be highly sensitive and specific. In a landmark Icelandic study, linkage was established between stroke and a locus on chromosome 5q12 designated STRK1. Association studies continue to identify polymorphisms that predispose to stroke and to markers for cerebrovascular atherosclerosis, such as intima-media thickness. Intense interest now surrounds genes involved in inflammation, including genes that encode for the interleukin-1 receptor antagonist and paraoxonase-1. In the foreseeable future, prevention, diagnosis, and treatment will incorporate genetic data to refine and individualize management of cerebrovascular disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1528-4042
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
420-6
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15324609-Anemia, Sickle Cell,
pubmed-meshheading:15324609-Arteriosclerosis,
pubmed-meshheading:15324609-Dementia, Multi-Infarct,
pubmed-meshheading:15324609-Genetic Linkage,
pubmed-meshheading:15324609-Genetic Markers,
pubmed-meshheading:15324609-Genetic Predisposition to Disease,
pubmed-meshheading:15324609-Homocysteine,
pubmed-meshheading:15324609-Humans,
pubmed-meshheading:15324609-Lipid Metabolism,
pubmed-meshheading:15324609-Lipoproteins,
pubmed-meshheading:15324609-MELAS Syndrome,
pubmed-meshheading:15324609-Mutation,
pubmed-meshheading:15324609-Polymorphism, Genetic,
pubmed-meshheading:15324609-Stroke
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pubmed:year |
2004
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pubmed:articleTitle |
New advances in identifying genetic anomalies in stroke-prone probands.
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pubmed:affiliation |
Department of Neurology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL 32224, USA. meschia.james@mayo.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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