246 top medical experts on 22q11 Deletion Syndrome across 27 countries and 21 U.S. states, including 81 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 22q11 Deletion Syndrome: Condition with a variable constellation of phenotypes due to deletion polymorphisms at chromosome location 22q11. It encompasses several syndromes with overlapping abnormalities including the digeorge syndrome, velocardiofacial syndrome, and conotruncal amomaly face syndrome. In addition, variable developmental problems and schizoid features are also associated with this syndrome. (From BMC Med Genet. 2009 Feb 25;10:16) Not all deletions at 22q11 result in the 22q11deletion syndrome.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Congenital Heart Defects (4,797), Multiple Abnormalities (3,208), Craniofacial Abnormalities (2,386), Chromosome Disorders (2,206), Hypoparathyroidism (3,365), Lymphatic Abnormalities (1,574) and Narrower Categories: DiGeorge Syndrome (1,129).
  4. Clinical Trials ClinicalTrials.gov : at least 6 including 2 Completed, 2 Recruiting


  

        

                    


    Computing Expert Listing ...

);