Source:http://linkedlifedata.com/resource/pubmed/id/17571027
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2007-6-15
|
pubmed:abstractText |
Spinocerebellar ataxia type 7 (SCA 7) is a rare autosomal dominant neurodegenerative disorder (ADCA) caused by expansion of a highly unstable CAG repeat. Clinical features including progressive cerebellar, retinal degeneration and pyramidal signs. We report a patient with SCA 7 diagnosis revealed by progressive cerebellar ataxia and writer's cramp.
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0035-3787
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
163
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
589-91
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:17571027-Adult,
pubmed-meshheading:17571027-Botulinum Toxins, Type A,
pubmed-meshheading:17571027-Dystonic Disorders,
pubmed-meshheading:17571027-Humans,
pubmed-meshheading:17571027-Male,
pubmed-meshheading:17571027-Nerve Tissue Proteins,
pubmed-meshheading:17571027-Neuromuscular Agents,
pubmed-meshheading:17571027-Spinocerebellar Ataxias
|
pubmed:year |
2007
|
pubmed:articleTitle |
[Writer's cramp secondary to spinocerebellar ataxia type 7].
|
pubmed:affiliation |
Service de Neurologie - Centre Hospitalier Universitaire de Nîmes, Hôpital Caremeau 30029 Nîmes.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|