rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8973
|
pubmed:dateCreated |
1995-9-14
|
pubmed:abstractText |
Glomerulonephritis with proteinuria of sufficient degree to manifest the nephrotic syndrome followed aplastic crises induced by human parvovirus (B19) in seven patients with homozygous sickle-cell disease, within 7 days in five patients and 6-7 weeks in two. Segmental proliferative glomerulonephritis was found in all four patients who underwent acute renal biopsies and focal segmental glomerulosclerosis was found in the fifth patient who had a biopsy 4 months later. One patient recovered completely, one died in chronic renal failure after 3 months, and the others had impaired creatinine clearance, four with continuing proteinuria.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0140-6736
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
19
|
pubmed:volume |
346
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
475-6
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:7637482-Adolescent,
pubmed-meshheading:7637482-Adult,
pubmed-meshheading:7637482-Anemia, Sickle Cell,
pubmed-meshheading:7637482-Antibodies, Viral,
pubmed-meshheading:7637482-Biopsy,
pubmed-meshheading:7637482-Child,
pubmed-meshheading:7637482-DNA, Viral,
pubmed-meshheading:7637482-Erythema Infectiosum,
pubmed-meshheading:7637482-Female,
pubmed-meshheading:7637482-Glomerulosclerosis, Focal Segmental,
pubmed-meshheading:7637482-Homozygote,
pubmed-meshheading:7637482-Humans,
pubmed-meshheading:7637482-Kidney,
pubmed-meshheading:7637482-Male,
pubmed-meshheading:7637482-Nephrotic Syndrome,
pubmed-meshheading:7637482-Parvovirus B19, Human,
pubmed-meshheading:7637482-Proteinuria
|
pubmed:year |
1995
|
pubmed:articleTitle |
Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease.
|
pubmed:affiliation |
MRC Laboratories, Jamaica.
|
pubmed:publicationType |
Journal Article,
Case Reports
|