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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1997-8-5
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pubmed:abstractText |
Fabry's disease is a hereditary sex-linked sphinglopidosis characterised by abnormal cellular lipid overload in most organs due to deficiencies in enzymes implicated in the catabolism of certain neutral glycolipids. There are two main clinical forms; cardiovascular manifestations usually congestive cardiac failure, and renal manifestations progressing to renal failure and death due to uraemic coma. The authors report a case presenting with juvenile, symptomatic complete infrahisian atrioventricular block. They describe the different cardiovascular complications of Fabry's disease from a review of the medical literature.
|
pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0003-9683
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
90
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
393-7
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pubmed:dateRevised |
2009-2-13
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pubmed:meshHeading |
pubmed-meshheading:9232078-Cardiovascular Diseases,
pubmed-meshheading:9232078-Diagnosis, Differential,
pubmed-meshheading:9232078-Electrocardiography,
pubmed-meshheading:9232078-Fabry Disease,
pubmed-meshheading:9232078-Heart Block,
pubmed-meshheading:9232078-Humans,
pubmed-meshheading:9232078-Leukocytes,
pubmed-meshheading:9232078-Male,
pubmed-meshheading:9232078-Middle Aged,
pubmed-meshheading:9232078-Syncope,
pubmed-meshheading:9232078-alpha-Galactosidase
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pubmed:year |
1997
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pubmed:articleTitle |
[Complete atrioventricular block disclosing Fabry's disease].
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pubmed:affiliation |
Service de cardiologie et urgences cardiovasculaires, center hospitalier de Lagny-Marne-la-Vailée.
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pubmed:publicationType |
Journal Article,
English Abstract,
Review,
Case Reports
|