Source:http://linkedlifedata.com/resource/pubmed/id/17514630
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-5-21
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pubmed:abstractText |
A 17-year-old boy was admitted to the hospital twice in a year for 2 episodes of hemolytic uremic syndrome (HUS). During these 2 HUS episodes he had diarrhea, decreased serum complement, decreased total protein and decreased serum albumin concentrations. We suggest that protein-losing enteropathy and hypocomplementemia due to intestinal lymphangiectasia is may be a rare cause of atypical HUS.
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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:issn |
1121-8428
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
246-9
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pubmed:meshHeading |
pubmed-meshheading:17514630-Adolescent,
pubmed-meshheading:17514630-Complement System Proteins,
pubmed-meshheading:17514630-Hemolytic-Uremic Syndrome,
pubmed-meshheading:17514630-Humans,
pubmed-meshheading:17514630-Lymphangiectasis, Intestinal,
pubmed-meshheading:17514630-Male,
pubmed-meshheading:17514630-Protein-Losing Enteropathies,
pubmed-meshheading:17514630-Recurrence
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pubmed:articleTitle |
Recurrent hemolytic uremic syndrome associated with intestinal lymphangiectasia.
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pubmed:affiliation |
Department of Pediatric Nephrology, Gazi University, Besevler, Ankara, Turkey. suleymankalman@yahoo.com
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pubmed:publicationType |
Journal Article,
Case Reports
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