333 top medical experts on Fanconi Syndrome across 41 countries and 22 U.S. states, including 184 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Errors Renal Tubular Transport (984).
  4. Clinical Trials ClinicalTrials.gov : at least 69 including 5 Active, 33 Completed, 12 Recruiting
  5. Synonyms: De Toni-Debre-Fanconi Syndrome,  Lignac-Fanconi Syndrome,  Proximal Renal Tubular Dysfunction,  Renal Fanconi Syndrome


  

        

                    


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