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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1981-12-15
|
| pubmed:abstractText |
A male infant with clinical and radiological manifestations of hypophosphatemic rickets is presented. He had dysfunction of the renal tubular mechanisms of reabsorption manifested by: glycosuria, hyperaminoaciduria, hyperphosphaturia and high alkaline phosphatase plasma levels; associated with hepatic cirrhosis. Biochemical screening discarded most of the main known causes of Toni-Debré-Fanconi syndrome. Unfortunately, due to the low incidence of the syndrome and the patient's death, it was impossible to reach an accurate diagnosis. A review of the syndrome is presented.
|
| pubmed:language |
spa
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0539-6115
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
38
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
169-75
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:7284065-Fanconi Syndrome,
pubmed-meshheading:7284065-Glycosuria,
pubmed-meshheading:7284065-Humans,
pubmed-meshheading:7284065-Infant,
pubmed-meshheading:7284065-Kidney Tubules, Proximal,
pubmed-meshheading:7284065-Liver Cirrhosis,
pubmed-meshheading:7284065-Male,
pubmed-meshheading:7284065-Phosphates,
pubmed-meshheading:7284065-Rickets
|
| pubmed:articleTitle |
[Fanconi syndrome with hepatic cirrhosis. Presentation of a case].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|