202 top medical experts on 1 X-linked Charcot-Marie-Tooth disease across 21 countries and 9 U.S. states, including 31 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 1 X-linked Charcot-Marie-Tooth disease: X-linked Charcot-Marie-Tooth disease type 1 is a rare, genetic, peripheral sensorimotor neuropathy characterized by an X-linked dominant inheritance pattern and the childhood-onset (within the first decade in males) of progressive, distal, moderate to severe muscle weakness and atrophy in lower extremities and intrinsic hand muscles, pes cavus, bilateral foot drop, reduced or absent tendon reflexes, as well as mild to moderate sensory impairment in lower extremities. Females tend to have milder manifestations or may be asymptomatic. Sensorineural deafness and central nervous system involvement 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: CMTX 1,  1 X-Linked Charcot-Marie-Tooth Neuropathy,  X-linked Charcot-Marie-Tooth peroneal muscular atrophy,  Cmtx1,  X-linked HMSN,  X-linked Hereditary motor and sensory neuropathy


  

        

                    


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