Table 1.
Primary Fanconi syndrome |
NaPi-II cotransporter mutation |
EHHADH gene mutation |
HNF4A gene (R76W) mutation |
Fanconi syndrome associated with inherited systemic diseases |
Cystinosis |
Galactosemia |
Hereditary fructose intolerance |
Tyrosinemia |
Lowe syndrome |
Alport syndrome |
Wilson disease |
Mitochondrial disorders |
Lysinuric protein intolerance |
Fanconi–Bickel syndrome |