205 top medical experts on Chromosome 22q11.2 Microduplication Syndrome across 20 countries and 15 U.S. states, including 29 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Chromosome 22q11.2 Microduplication Syndrome: A rare chromosomal anomaly characterized by an extremely variable clinical phenotype and may include heart defects, urogenital abnormalities, velopharyngeal insufficiency with or without cleft palate, and ranging from multiple defects to mild learning difficulties with some individuals being essentially normal.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 22q11.2 Duplication,  Chromosome 22q11.2 Duplication Syndrome


  

        

                    


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