204 top medical experts on Cohen syndrome across 21 countries and 6 U.S. states, including 41 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Cohen syndrome: A rare developmental defect during embryogenesis characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: and Prominent Incisors Obesity Hypotonia,  Mirhosseini-Holmes-Walton syndrome,  Norio Syndrome,  Obesity-Hypotonia Syndrome,  Pepper syndrome,  Prominent Incisors-Obesity-Hypotonia Syndrome,  Retinopathy pigmentary mental retardation,  And Mental Retardation Pigmentary Retinopathy


  

        

                    


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