Charcot Marie Tooth Disease
As stated on WebMD[1], Charcot-Marie-Tooth Disease (abbreviated CMT) is "a group of disorders in which the motor and/or sensory peripheral nerves are affected, resulting in muscle weakness and atrophy, as well as sensory loss. These manifestions occur first in the distal legs and later in the hands. The nerve cells in individuals with this disorder are not able to send electrical signals properly because of abnormalities in the nerve axon or abnormalities in the insulation (myelin) around the axon. Specific gene mutations are responsible for the abnormal function of the peripheral nerves. Charcot Marie Tooth disease can be inherited in an autosomal dominant, autosomal recessive or X-linked mode of inheritance." It is also known as Hereditary Motor and Sensory Neuropathy (HMSN) or Peroneal Muscular Atrophy (PMA)[2], but the disease in general is accepted by the community who has it as not receiving a great deal of publicity[3], they say things like "what bothers me is when I tell a doctor about CMT.....and get that blank, dull look.....they have no clue."[4] -tickyul, YouTube user. John 3:17