Fanconi Syndrome
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.
Year introduced: 1965
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Subheadings:
Tree Number(s): C12.050.351.968.419.815.450, C12.200.777.419.815.450, C12.950.419.815.450, C16.320.831.450
MeSH Unique ID: D005198
Entry Terms:
- Syndrome, Fanconi
- Proximal Renal Tubular Dysfunction
- Fanconi Syndrome without Cystinosis
- Fanconi Renotubular Syndrome
- Renotubular Syndrome, Fanconi
- Syndrome, Fanconi Renotubular
- 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 Bickel Syndrome
- Bickel Syndrome, Fanconi
- Syndrome, Fanconi Bickel
- Glycogen Storage Disease XI
- Glycogenosis, Fanconi Type
- Fanconi Type Glycogenosis
- Fanconi-Bickel Syndrome
- Fanconi-Bickel Syndromes
- Syndrome, Fanconi-Bickel
- Syndromes, Fanconi-Bickel
- Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
- 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
- Pseudo-Phlorizin Diabetes
- Diabete, Pseudo-Phlorizin
- Diabetes, Pseudo-Phlorizin
- Pseudo-Phlorizin Diabete
- Pseudo Phlorizin Diabetes
- Toni-Debre-Fanconi Syndrome
- De Toni-Debre-Fanconi Syndrome
- Neonatal De Toni-Debre-Fanconi Syndrome
- Primary Toni-Debre-Fanconi Syndrome
- Idiopathic De Toni-Debre-Fanconi Syndrome
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