Fanconi Syndrome


Adult Fanconi Syndrome

Bickel Syndrome, Fanconi

De Toni-Debre-Fanconi Syndrome

Diabete, Pseudo-Phlorizin

Diabetes, Pseudo-Phlorizin

Fanconi Bickel Syndrome

Fanconi Renotubular Syndrome

Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance

Fanconi Syndrome without Cystinosis

Fanconi Syndrome, Adult

Fanconi Syndrome, Renal

Fanconi Type Glycogenosis

Fanconi-Bickel Syndrome

Fanconi-Bickel Syndromes

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

Idiopathic De Toni-Debre-Fanconi Syndrome

Lignac Fanconi Syndrome

Lignac-Fanconi Syndrome

Luder Sheldon Syndrome

Luder-Sheldon Syndrome

Neonatal De Toni-Debre-Fanconi Syndrome

Primary Toni-Debre-Fanconi Syndrome

Proximal Renal Tubular Dysfunction

Pseudo Phlorizin Diabetes

Pseudo-Phlorizin Diabete

Pseudo-Phlorizin Diabetes

Renal Fanconi Syndrome

Renotubular Syndrome, Fanconi

Syndrome, Adult Fanconi

Syndrome, Fanconi

Syndrome, Fanconi Bickel

Syndrome, Fanconi Renotubular

Syndrome, Fanconi-Bickel

Syndrome, Lignac-Fanconi

Syndrome, Luder-Sheldon

Syndrome, Renal Fanconi

Syndromes, Fanconi-Bickel

Toni-Debre-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.