110 top medical experts on Type 1A Vitamin D Hydroxylation-Deficient Rickets across 10 countries and 2 U.S. states, including 10 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type 1A Vitamin D Hydroxylation-Deficient Rickets: An early-onset hereditary vitamin D metabolism disorder characterized by severe hypocalcemia leading to osteomalacia and rachitic bone deformations, and moderate hypophosphatemia.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Selective 25-Hydroxyvitamin D3 Deficiency 1-Alpha,  1-Alpha-Hydroxylase Deficiency,  25-Hydroxycholecalciferol-1-Hydroxylase Deficiency,  PDDR1A,  Type IA Pseudovitamin D-Deficiency Rickets,  VDDR1A,  Type 1 Vitamin D Dependency,  Type 1A Vitamin D-Dependent Rickets


  

        

                    


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