309 top medical experts on Multiple Hereditary Exostoses across 42 countries and 27 U.S. states, including 169 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Multiple Hereditary Exostoses: Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Osteochondromatosis (77), Exostoses (819), Hereditary Neoplastic Syndromes (1,826).
  4. Clinical Trials ClinicalTrials.gov : at least 7 including 2 Completed, 2 Recruiting
  5. Synonyms: Hereditary Deforming Chondrodysplasia,  Diaphyseal Aclasis,  Familial Exostoses,  Hereditary Multiple Exostoses,  Multiple Exostoses,  Multiple Cartilaginous Exostoses,  Hereditary Multiple Exostoses,  Multiple Osteochondromas


  

        

                    


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