213 top medical experts on Familial Hypophosphatemia across 23 countries and 15 U.S. states, including 67 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial Hypophosphatemia: An inherited condition of abnormally low serum levels of phosphates (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the proximal renal tubules. This leads to phosphaturia, hypophosphatemia, and disturbances of cellular and organ functions such as those in X-linked hypophosphatemic rickets; osteomalacia; and fanconi syndrome.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hypophosphatemia (2,411), Inborn Errors Renal Tubular Transport (984), Inborn Errors Metal Metabolism (445) and Narrower Categories: Familial Hypophosphatemic Rickets (1,590).
  4. Clinical Trials ClinicalTrials.gov : at least 3 including 2 Completed


  

        

                    


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