393 top medical experts on Williams Syndrome across 32 countries and 32 U.S. states, including 273 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Williams Syndrome: A disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, including the elastin gene. Clinical manifestations include supravalvular aortic stenosis; mental retardation; elfin facies; impaired visuospatial constructive abilities; and transient hypercalcemia in infancy. The condition affects both sexes, with onset at birth or in early infancy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Chromosome Disorders (2,206), Intellectual Disability (5,155), Supravalvular Aortic Stenosis (591).
  4. Clinical Trials ClinicalTrials.gov : at least 21 including 1 Active, 8 Completed, 8 Recruiting
  5. Synonyms: Williams Contiguous Gene Syndrome


  

        

                    


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