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As Fine described, "The result is a proximal renal tubular acidosis (usually hypokalemic) with hypophosphatemia, glucosuria, and aminoaciduria (Fanconi syndrome)" (3).
Excess production of FGF23 epidermal naevus syndrome Abnormalities of renal Na dependent P co-transporter: Hereditary hypophosphataemic Inactivating mutation in rickets with hypercalciuria SLC34A3 gene Other defects of renal tubular function: Fanconi syndrome Proximal renal tubular acidosis Distal renal tubular acidosis FGF23, fibroblast growth factor 23; PHEX, phosphate regulating gene with homologies to endopeptidases on the X chromosome; DMP1, dentin matrix protein 1; FRP4, Frizzled-related protein 4; MEPE, matrix extracellular phosphoglycoprotein; SLC34A3, type IIc sodium- phosphate co-transporter