334 top medical experts on Hereditary Sensory and Motor Neuropathy across 41 countries and 18 U.S. states, including 150 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Sensory and Motor Neuropathy: A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include hmsns I-VII. hmsn I and II both refer to charcot-marie-tooth disease. hmsn III refers to hypertrophic neuropathy of infancy. hmsn IV refers to refsum disease. hmsn V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see spastic paraplegia, hereditary). hmsn VI refers to hmsn associated with an inherited optic atrophy (optic atrophies, hereditary), and hmsn VII refers to hmsn associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Polyneuropathies (1,469), Nervous System Heredodegenerative Disorders (865), Nervous System Malformations (1,185) and Narrower Categories: Alstrom Syndrome (569), Charcot-Marie-Tooth Disease (1,872), Giant Axonal Neuropathy (278), Hereditary Spastic Paraplegia (1,244), Refsum Disease (141).
  4. Clinical Trials ClinicalTrials.gov : at least 79 including 4 Active, 36 Completed, 17 Recruiting
  5. Synonyms: Dejerine-Sottas Disease,  HMSN,  HMSN Type III,  HMSN Type VII,  Hereditary Motor and Sensory Neuropathies,  Motor and Sensory Neuropathy Type III Hereditary,  Motor and Sensory Neuropathy Type VII Hereditary,  Hereditary Motor and Sensory Neuropathies


  

        

                    


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