Source:http://linkedlifedata.com/resource/pubmed/id/20140769
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2010-5-21
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pubmed:abstractText |
Metabolic disorders are often encountered in clinical practice. Some of these diseases are associated with dermatological and musculoskeletal manifestations. Familial hypercholesterolemia is a disorder of lipoprotein metabolism characterized by elevated cholesterol, low-density lipoprotein cholesterol, xanthomas and early onset atherosclerosis. Tendinitis and arthritis have been rarely reported in patients with familial hypercholesterolemia. Here is presented a case of a young girl with migratory polyarthritis, who was diagnosed as probable homozygote familial hypercholesterolemia with hypercholesterolemic arthritis. A proper knowledge of cutaneous manifestations helps to identify patients at risk, establish the underlying diagnosis, and start early and effective therapy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0973-7693
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
77
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
329-31
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Migratory polyarthritis in familial hypercholesterolemia (type IIa hyperlipoproteinemia).
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pubmed:affiliation |
Department of Medicine, Midnapore Medical College, Paschim Medinipur, West Bengal, India. docparthapc@yahoo.co.in
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pubmed:publicationType |
Journal Article,
Case Reports
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