Source:http://linkedlifedata.com/resource/pubmed/id/14626738
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2003-11-20
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pubmed:abstractText |
The authors report the case of a 21 year old woman admitted to hospital for congestive cardiac failure due to concentric hypertrophic cardiomyopathy. Echocardiography showed severe systolo-diastolic left ventricular dysfunction without obstruction to ejection. Neurological examination showed a stato-kinetic cerebellar syndrome, a posterior radiculo-cordonal syndrome and a dysmorphic syndrome which characterise Friedreich's disease. In the light of this case and a review of the literature, the authors underline the rarity of cardiomyopathy in Friedreich's disease, its particular presentation and its poor prognostic significance in this disease.
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pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0003-9683
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
140-3
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pubmed:dateRevised |
2009-2-13
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pubmed:meshHeading | |
pubmed:year |
2003
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pubmed:articleTitle |
[Hypertrophic cardiomyopathy disclosing Friedreich's disease. Report of a case].
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pubmed:affiliation |
Service de cardiologie, CHU lbn Rochd, Casablanca, Maroc. adarif54@Hotmail.com
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pubmed:publicationType |
Journal Article,
English Abstract,
Review,
Case Reports
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