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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4 Pt 1
|
pubmed:dateCreated |
1992-4-30
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pubmed:abstractText |
We report the case of a patient with infantile nephropathic cystinosis who required renal transplantation at age 30 months. Exhaustive evaluation did not identify a cause of progressive renal failure other than cystinosis. The patient's genetic lesion was allelic with those of other patients with cystinosis; fusion of this patient's fibroblasts with fibroblasts from another patient with infantile nephropathic cystinosis did not demonstrate complementation of the biochemical defect.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0022-3476
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
120
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
575-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1552398-Clone Cells,
pubmed-meshheading:1552398-Cystine,
pubmed-meshheading:1552398-Cystinosis,
pubmed-meshheading:1552398-Female,
pubmed-meshheading:1552398-Fibroblasts,
pubmed-meshheading:1552398-Humans,
pubmed-meshheading:1552398-Infant,
pubmed-meshheading:1552398-Kidney,
pubmed-meshheading:1552398-Kidney Failure, Chronic
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pubmed:year |
1992
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pubmed:articleTitle |
Early occurrence of end-stage renal disease in a patient with infantile nephropathic cystinosis.
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pubmed:affiliation |
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports,
Research Support, Non-U.S. Gov't
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