16 top medical experts on Optic atrophy polyneuropathy deafness across 1 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Optic atrophy polyneuropathy deafness: A rare form of X-linked Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by infancy- to childhood-onset of: 1) progressive distal muscle weakness and atrophy (first appearing and more prominent in the lower extremities than the upper) which usually manifests with foot drop and gait disturbance, 2) bilateral, profound, prelingual sensorineural hearing loss and 3) progressive optic neuropathy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: 5 X-Linked Recessive Charcot-Marie-Tooth Disease,  5 X-Linked Recessive Charcot-Marie-Tooth Neuropathy,  Familial opticoacoustic nerve degeneration and polyneuropathy,  autosomal recessive and peripheral neuropathy hearing loss Optic atrophy,  and distal neurogenic amyotrophy neural deafness Optic atrophy,  and deafness polyneuropathy Optic atrophy,  sensorineural hearing loss and polyneuropathy Optic atrophy,  Rosenberg Chutorian syndrome,  Rosenberg-Chutorian Syndrome


  

        

                    


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