44 top medical experts on Type V Distal Hereditary Motor Neuronopathy across 4 countries and 4 U.S. states, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type V Distal Hereditary Motor Neuronopathy: A rare autosomal dominant distal hereditary motor neuropathy disease characterized by muscle weakness and wasting predominantly affecting the hands, in particular the thenar and first dorsal interosseus muscles, and/or marked foot deformity and gait disturbance. Sensation is normal, although reduced response to vibration has been described. The disease is slowly progressive with an age of onset within the first few decades of life.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: DHMN V,  DHMN5,  DSMAV,  Dhmn-V,  Type V Distal Hereditary Motor Neuropathy,  Type V Distal Spinal Muscular Atrophy,  HMN V,  HMN5,  Type V Distal Hereditary Motor Neuropathy,  Distal Type V Spinal Muscular Atrophy,  Type V Distal Spinal Muscular Atrophy,  With Upper Limb Predominance Distal Spinal Muscular Atrophy


  

        

                    


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