203 top medical experts on Giant Axonal Neuropathy across 18 countries and 10 U.S. states, including 34 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Giant Axonal Neuropathy: Rare autosomal recessive disorder of intermediate filament proteins. The disease is caused by mutations in the gene that codes gigaxonin protein. The mutations result in disorganization of axonal neurofilament proteins, formation of the characteristic giant axons, and progressive neuropathy. The clinical features of the disease include early-onset progressive peripheral motor and sensory neuropathies often associated with central nervous system involvement (intellectual disability, seizures, dysmetria, and congenital nystagmus).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Peripheral Nervous System Diseases (3,813), Hereditary Sensory and Motor Neuropathy (1,703).
  4. Clinical Trials ClinicalTrials.gov : at least 2 including 1 Recruiting
  5. Synonyms: Giant Axonal Neuropathy (GAN),  Giant Axonal Neuropathy 1,  Giant Axonal Neuropathy 1 (GAN1)


  

        

                    


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