205 top medical experts on Chromosome 17q21.31 Deletion Syndrome across 17 countries and 12 U.S. states, including 16 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Chromosome 17q21.31 Deletion Syndrome: A rare multisystem disorder characterized by neonatal/childhood hypotonia, mild to moderate developmental delay or intellectual disability, epilepsy, dysmorphic facial features, hypermetropia, congenital heart anomalies, congenital renal/urologic anomalies, musculoskeletal problems, and a friendly/amiable disposition.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 17q21.31 Deletion Syndrome,  17q21.31 Microdeletion Syndrome,  Chromosome 17q21.31 Microdeletion Syndrome,  Koolen Syndrome,  Koolen-De Vries Syndrome,  Microdeletion 17q21.31 Syndrome,  Monosomy 17q21.31


  

        

                    


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