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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1989-7-28
|
| pubmed:abstractText |
A review of 130 children with persistent microhematuria showed that the most common abnormality was a form of hereditary nephritis for wich we propose the term 'familial thin basement membrane nephropathy' (FTBMN). This lesion is not as severe as that of Alport's syndrome but carries a guarded prognosis. Family histories, urinalyses and audiograms systematically done on parents and other relatives show that FTBMN may be present in as many as 39% of children with persistent microhematuria and that careful family studies identify children likely to have this lesion.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0028-2766
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
51
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
502-8
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:2739828-Adolescent,
pubmed-meshheading:2739828-Basement Membrane,
pubmed-meshheading:2739828-Child,
pubmed-meshheading:2739828-Child, Preschool,
pubmed-meshheading:2739828-Female,
pubmed-meshheading:2739828-Follow-Up Studies,
pubmed-meshheading:2739828-Hematuria,
pubmed-meshheading:2739828-Humans,
pubmed-meshheading:2739828-Infant,
pubmed-meshheading:2739828-Male,
pubmed-meshheading:2739828-Nephritis, Hereditary,
pubmed-meshheading:2739828-Retrospective Studies
|
| pubmed:year |
1989
|
| pubmed:articleTitle |
Familial thin basement membrane nephropathy in children with asymptomatic microhematuria.
|
| pubmed:affiliation |
Schneider Children's Hospital of Long Island Jewish Medical Center, New Hyde Park, N.Y.
|
| pubmed:publicationType |
Journal Article
|