288 top medical experts on Hereditary Sensory and Autonomic Neuropathies across 40 countries and 21 U.S. states, including 117 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Sensory and Autonomic Neuropathies: A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is dysautonomia, familial. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
  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: Familial Dysautonomia (435).
  4. Clinical Trials ClinicalTrials.gov : at least 6 including 2 Completed, 2 Recruiting
  5. Synonyms: HSAN,  HSAN Type I,  HSAN Type II,  HSAN Type IV,  HSAN Type V,  HSN Type I,  HSN Type II,  Congenital Insensitivity to Pain with Anhidrosis,  Congenital Pain Insensitivity with Anhidrosis,  Hereditary Sensory Neuropathy


  

        

                    


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