249 top medical experts on Neuroaxonal Dystrophies across 30 countries and 22 U.S. states, including 72 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Neuroaxonal Dystrophies: A nonspecific term referring both to the pathologic finding of swelling of distal portions of axons in the brain and to disorders which feature this finding. Neuroaxonal dystrophy is seen in various genetic diseases, vitamin deficiencies, and aging. Infantile neuroaxonal dystrophy is an autosomal recessive disease characterized by arrested psychomotor development at 6 months to 2 years of age, ataxia, brain stem dysfunction, and quadriparesis. Juvenile and adult forms also occur. Pathologic findings include brain atrophy and widespread accumulation of axonal spheroids throughout the neuroaxis, peripheral nerves, and dental pulp. (From Davis & Robertson, Textbook of Neuropathology, 2nd ed, p927)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Brain Diseases (4,643) and Narrower Categories: Pantothenate Kinase-Associated Neurodegeneration (774).
  4. Clinical Trials ClinicalTrials.gov : at least 5 including 1 Active, 2 Completed
  5. Synonyms: Juvenile Neuroaxonal Dystrophy,  Seitelberger's Disease


  

        

                    


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