37 top medical experts on Type 2A2 Axonal Charcot-Marie-Tooth Disease across 5 countries and 2 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type 2A2 Axonal Charcot-Marie-Tooth Disease: A subtype of Autosomal dominant Charcot-Marie-Tooth disease type 2 characterized by the childhood onset of distal weakness and areflexia (with earlier and more severe involvement of the lower extremities), reduced sensory modalities (primarily pain and temperature sensation), foot deformities, postural tremor, scoliosis and contractures. Optic atrophy, vocal cord palsy with dysphonia, sensorineural hearing loss, spinal cord abnormalities and hydrocephalus have also been reported.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: CMT2A2,  Type 2A2 Autosomal Dominant Axonal Charcot-Marie-Tooth Disease,  Type 2A2 Neuronal Charcot-Marie-Tooth Disease,  Type 2A2 Charcot-Marie-Tooth Neuropathy,  HMSN2A2,  HMSNIIA2,  Hereditary Motor And Sensory Neuropathy IIA2


  

        

                    


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