"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
|
| MeSH Number(s) |
C12.777.419.815.450 C13.351.968.419.815.450 C16.320.565.861.450 C18.452.648.861.450
|
| Concept/Terms |
Fanconi Syndrome- Fanconi Syndrome
- Syndrome, Fanconi
- Proximal Renal Tubular Dysfunction
Toni-Debre-Fanconi Syndrome- Toni-Debre-Fanconi Syndrome
- Primary Toni-Debre-Fanconi Syndrome
- Neonatal De Toni-Debre-Fanconi Syndrome
- De Toni-Debre-Fanconi Syndrome
- Idiopathic De Toni-Debre-Fanconi Syndrome
Fanconi Bickel Syndrome- Fanconi Bickel Syndrome
- Bickel Syndrome, Fanconi
- Syndrome, Fanconi Bickel
- Fanconi-Bickel Syndrome
- Fanconi-Bickel Syndromes
- Syndrome, Fanconi-Bickel
- Syndromes, Fanconi-Bickel
- Glycogen Storage Disease XI
- Pseudo-Phlorizin Diabetes
- Diabete, Pseudo-Phlorizin
- Diabetes, Pseudo-Phlorizin
- Pseudo Phlorizin Diabetes
- Pseudo-Phlorizin Diabete
- Hepatic Glycogenosis with Amino Aciduria and Glucosuria
- Hepatic Glycogenosis with Fanconi Nephropathy
- Hepatorenal Glycogenosis with Renal Fanconi Syndrome
- Lignac-Fanconi Syndrome
- Lignac Fanconi Syndrome
- Syndrome, Lignac-Fanconi
- Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
- Glycogenosis, Fanconi Type
- Fanconi Type Glycogenosis
Fanconi Syndrome without Cystinosis- Fanconi Syndrome without Cystinosis
- Renal Fanconi Syndrome
- Fanconi Syndrome, Renal
- Syndrome, Renal Fanconi
- Luder-Sheldon Syndrome
- Luder Sheldon Syndrome
- Syndrome, Luder-Sheldon
- Adult Fanconi Syndrome
- Fanconi Syndrome, Adult
- Syndrome, Adult Fanconi
- Fanconi Renotubular Syndrome
- Renotubular Syndrome, Fanconi
- Syndrome, Fanconi Renotubular
|
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,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Fanconi Syndrome" by people in Profiles.
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Newborn Screening: Review of its Impact for Cystinosis. Cells. 2022 03 25; 11(7).
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Management of bone disease in cystinosis: Statement from an international conference. J Inherit Metab Dis. 2019 09; 42(5):1019-1029.
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Renal Fanconi syndrome with meropenem/amoxicillin-clavulanate during treatment of extensively drug-resistant tuberculosis. Eur Respir J. 2017 12; 50(6).
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Fanconi Anemia and Fanconi Syndrome: Time to Correct the Misnomers. J Pediatr Hematol Oncol. 2016 10; 38(7):585.
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A Rare Case of Acquired Fanconi's Syndrome With Monoclonal Gammopathy in an Infant. J Clin Lab Anal. 2016 Sep; 30(5):510-2.
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Nephropathic cystinosis: an international consensus document. Nephrol Dial Transplant. 2014 Sep; 29 Suppl 4:iv87-94.
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Cystinosis in non-caucasian children. Johns Hopkins Med J. 1982 Sep; 151(3):117-21.
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Proximal tubular necrosis associated with maleic acid administration to the rat. Lab Invest. 1982 Jan; 46(1):79-88.
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Maleic acid-induced impaired conversion of 25(OH)D3 to 1,25(OH)2D3: implications for Fanconi's syndrome. Kidney Int. 1977 Oct; 12(4):244-52.
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Ocular manifestations of de Tonifanconi syndrome with cystine storage disease. South Med J. 1966 Jan; 59(1):33-40.