13 top medical experts on RHYNS syndrome across 2 countries and 1 U.S. states. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. RHYNS syndrome: A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia.
  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: Retinitis pigmentosa syndrome,  and mild Skeletal dysplasia Nephronophthisis HYpopituitarism Retinitis pigmentosa


  

        

                    


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