201 top medical experts on Camurati-Engelmann Syndrome across 22 countries and 8 U.S. states, including 28 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Camurati-Engelmann Syndrome: An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes transforming growth factor beta1 are one cause of this disorder.
  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 Genetic Diseases (2,477), Osteochondrodysplasias (1,587).
  4. Synonyms: Progressive Diaphyseal Dysplasia,  Engelmann's Disease


  

        

                    


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