 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
- Cystinosis, Nephropathic
- Cystinoses, Nephropathic
- Nephropathic Cystinoses
- De Toni-Debre-Fanconi Syndrome
- De Toni Debre Fanconi Syndrome
- Syndrome, De Toni-Debre-Fanconi
- Fanconi Bickel Syndrome
- Bickel Syndrome, Fanconi
- Syndrome, Fanconi Bickel
- Fanconi Renotubular Syndrome
- Syndrome, Fanconi Renotubular
- Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
- Glycogen Storage Disease XI
- Glycogenosis, Fanconi Type
- Fanconi Type Glycogenosis
- Hepatic Glycogenosis with Amino Aciduria and Glucosuria
- Hepatic Glycogenosis with Fanconi Nephropathy
- Hepatorenal Glycogenosis with Renal Fanconi Syndrome
- Idiopathic De Toni-Debre-Fanconi Syndrome
- Idiopathic De Toni Debre Fanconi Syndrome
- Lignac-Fanconi Syndrome
- Lignac Fanconi Syndrome
- Syndrome, Lignac-Fanconi
- Lysosomal Cystine Transport Protein, Defect Of
- 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
- Pseudo-Phlorizin Diabetes
- Diabete, Pseudo-Phlorizin
- Diabetes, Pseudo-Phlorizin
- Pseudo Phlorizin Diabetes
- Pseudo-Phlorizin Diabete
- Renal Fanconi Syndrome
- Toni-Debre-Fanconi Syndrome
- Toni Debre Fanconi Syndrome
- Cystinosin, Defect of
- Cystinosins, Defect of
- Defect of Cystinosin
- Defect of Cystinosins
Adult Fanconi Syndrome- Adult Fanconi Syndrome
- Fanconi Syndrome, Adult
- Syndrome, Adult Fanconi
- Fanconi Syndrome without Cystinosis
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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 UAMS Profiles 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 |
|---|
| 2022 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2006 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Fanconi Syndrome" by people in Profiles over the past ten years.
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Govindarajan S, Khandelwal P, Sharma S, Agarwala A, Sinha A, Hari P, Bagga A. Clinical Features and Genetic Sequencing of Children with Fanconi-Bickel Syndrome. Indian J Pediatr. 2023 02; 90(2):178-180.
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Wu X, Zhang L, Feng J, Mao YY, Cao XX, Zhou DB, Li J. Bortezomib-based chemotherapy can improve renal and tubular functions in patients with light chain-associated Fanconi syndrome. Ann Hematol. 2019 May; 98(5):1095-1100.
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