325 top medical experts on Familial Hypophosphatemic Rickets across 44 countries and 24 U.S. states, including 172 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial Hypophosphatemic Rickets: A hereditary disorder characterized by hypophosphatemia; rickets; osteomalacia; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Familial Hypophosphatemia (380), Hypophosphatemic Rickets (355).
  4. Clinical Trials ClinicalTrials.gov : at least 52 including 3 Active, 26 Completed, 16 Recruiting
  5. Synonyms: X-Linked Dominant Hypophosphatemic Rickets,  X-Linked Hypophosphatemic Rickets


  

        

                    


    Computing Expert Listing ...

);