573 top medical experts on Fragile X Syndrome across 42 countries and 35 U.S. states, including 449 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci fraxa or fraxe) and phenotypically by cognitive impairment, hyperactivity, seizures, language delay, and enlargement of the ears, head, and testes. intellectual disability occurs in nearly all males and roughly 50% of females with the full mutation of fraxa. (From Menkes, Textbook of Child Neurology, 5th ed, p226)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): X-Linked Mental Retardation (2,803), Sex Chromosome Disorders (669).
  4. Clinical Trials ClinicalTrials.gov : at least 85 including 3 Active, 49 Completed, 13 Recruiting
  5. Synonyms: FRAXA Syndrome,  FRAXE Syndrome,  Martin-Bell Syndrome


  

        

                    


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