10 top medical experts on Type I Distal Hereditary Motor Neuronopathy across 1 countries and 1 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type I Distal Hereditary Motor Neuronopathy: Distal hereditary motor neuropathy type 1 is a rare neuromuscular disease characterized by slowly-progressive lower limb muscular weakness and atrophy, without sensory impairment. Additional clinical features may include pes cavus, hammertoe and increased muscle tone.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: I Spinal Charcot-Marie-Tooth Disease,  Type I Distal Hereditary Motor Neuropathy,  I Autosomal Dominant Juvenile Distal Spinal Muscular Atrophy


  

        

                    


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