209 top medical experts on Langer-Giedion Syndrome across 30 countries and 5 U.S. states, including 21 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Langer-Giedion Syndrome: Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses. intellectual disability and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (exostoses, hereditary multiple).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Osteochondrodysplasias (1,587).
  4. Synonyms: Acrodysplasia V,  Giedion-Langer Syndrome,  Trichorhinophalangeal Syndrome Type II


  

        

                    


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