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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1985-8-20
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pubmed:abstractText |
Two children with nephrotic syndrome are described whose clinical course, initial response to steroids, and renal biopsies were consistent with a diagnosis of minimal lesion disease (MLD). Both children subsequently became resistant to steroids and repeat renal biopsies 7 and 8 years after initial biopsies showed membranous glomerulonephropathy (MGN). Explanations are suggested which may account for the occurrence of MLD followed by MGN in a single patient. These cases illustrate the necessity of performing repeat renal biopsies in patients with nephrotic syndrome if the clinical behavior and response to steroids are not typical for MLD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0301-0430
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
23
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
258-64
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:4006337-Basement Membrane,
pubmed-meshheading:4006337-Biopsy,
pubmed-meshheading:4006337-Child,
pubmed-meshheading:4006337-Child, Preschool,
pubmed-meshheading:4006337-Female,
pubmed-meshheading:4006337-Glomerular Mesangium,
pubmed-meshheading:4006337-Glomerulonephritis,
pubmed-meshheading:4006337-Humans,
pubmed-meshheading:4006337-Male,
pubmed-meshheading:4006337-Nephrosis, Lipoid
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pubmed:year |
1985
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pubmed:articleTitle |
Minimal lesion disease followed by membranous glomerulonephropathy in two children with nephrotic syndrome.
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pubmed:publicationType |
Journal Article,
Case Reports
|