622 top medical experts on Charcot-Marie-Tooth Disease across 48 countries and 31 U.S. states, including 499 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Charcot-Marie-Tooth Disease: A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (hmsn) types I and II. hmsn I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in hmsn II. (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): Hereditary Sensory and Motor Neuropathy (1,703).
  4. Clinical Trials ClinicalTrials.gov : at least 79 including 4 Active, 36 Completed, 17 Recruiting
  5. Synonyms: Peroneal Muscular Atrophy,  HMSN Type I,  HMSN Type II,  Hereditary Motor and Sensory-Neuropathy Type II,  and Sensory Neuropathy Type I Hereditary Motor,  Peroneal Muscular Atrophy,  Peroneal Muscular Atrophy,  Roussy-Levy Syndrome


  

        

                    


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