RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164067604 T1 De Toni Debré Fanconi Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164067604 RD 2024/10/16 AB A rare acquired or inherited condition involving a generalized transport defect within the proximal tubules of the kidneys leading to renal losses of glucose, phosphate, calcium, uric acid, amino acids, and bicarbonates. The clinical features include short stature, osteomalacia, and renal failure. Variants of Fanconi Syndrome are determined by how they affect the proximal tubule and its resulting complications. The loss of bicarbonate results in Type 2 Fanconi Syndrome often classified as “proximal renal tubular acidosis.” The loss of phosphate results in rickets and osteomalacia.