Fanconi Syndrome
"Fanconi Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A hereditary or acquired form of generalized dysfunction of the PROXIMAL KIDNEY TUBULE without primary involvement of the KIDNEY GLOMERULUS. It is usually characterized by the tubular wasting of nutrients and salts (GLUCOSE; AMINO ACIDS; PHOSPHATES; and BICARBONATES) resulting in HYPOKALEMIA; ACIDOSIS; HYPERCALCIURIA; and PROTEINURIA.
Descriptor ID |
D005198
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MeSH Number(s) |
C12.777.419.250 C12.777.419.815.450 C13.351.968.419.250 C13.351.968.419.815.450 C16.320.565.861.450 C18.452.648.861.450
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Concept/Terms |
Fanconi Syndrome- Fanconi Syndrome
- Syndrome, Fanconi
- Fanconi Renotubular Syndrome
- Syndrome, Fanconi Renotubular
- Idiopathic De Toni-Debre-Fanconi Syndrome
- Idiopathic De Toni Debre Fanconi Syndrome
- Lignac-Fanconi Syndrome
- Lignac Fanconi Syndrome
- Syndrome, Lignac-Fanconi
- Neonatal De Toni-Debre-Fanconi Syndrome
- Neonatal De Toni Debre Fanconi Syndrome
- Primary Toni-Debre-Fanconi Syndrome
- Primary Toni Debre Fanconi Syndrome
- Toni-Debre-Fanconi Syndrome, Primary
- Proximal Renal Tubular Dysfunction
- Renal Fanconi Syndrome
- Toni-Debre-Fanconi Syndrome
- Toni Debre Fanconi Syndrome
- Fanconi Bickel syndrome
- Fanconi syndrome with intestinal malabsorption and galactose intolerance
- Glycogen storage disease XI
- Glycogenosis, Fanconi type
- Hepatic glycogenosis with amino aciduria and glucosuria
- Hepatic glycogenosis with fanconi nephropathy
- Hepatorenal glycogenosis with renal Fanconi syndrome
- Pseudo-phlorizin diabetes
- De Toni-Debre-Fanconi Syndrome
- De Toni Debre Fanconi Syndrome
- Syndrome, De Toni-Debre-Fanconi
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Below are MeSH descriptors whose meaning is more general than "Fanconi Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Fanconi Syndrome".
This graph shows the total number of publications written about "Fanconi Syndrome" by people in this website by year, and whether "Fanconi Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2003 | 1 | 0 | 1 | 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fanconi Syndrome" by people in Profiles.
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Runde J, Rivera-Rivera E, Pompeii-Wolfe C, Clardy C, Sentongo T. Hypophosphatemia in a Malnourished Child: When Renal Fanconi Syndrome Does Not Stand for Refeeding Syndrome. JPEN J Parenter Enteral Nutr. 2019 01; 43(1):166-169.
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Ludwig M, Waldegger S, Nuutinen M, Bökenkamp A, Reissinger A, Steckelbroeck S, Utsch B. Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variant. Kidney Blood Press Res. 2003; 26(3):176-84.
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