This disease is the most commonly inherited neurological disorder affecting about one in 2,500 people.. ... Charcot-Marie-Tooth Association PO Box 105 Glenolden, PA 19036. Charcot-Marie-Tooth disease (CMT) is a spectrum of nerve disorders named after the three physicians who first described it in 1886 — Jean-Martin Charcot and Pierre Marie of France and Howard Henry Tooth of the United Kingdom. I reached out to Dr. Herrmann’s staff to see if I could participate in the research study. Learn more with CMTA educational materials: the CMTA Report, brochures, and CMTA webinars. Charcot-Marie-Tooth disease (CMT) is a group of inherited conditions that damage the peripheral nerves. Charcot-Marie-Tooth disease (CMT) is a group of rare and inherited conditions that damage the peripheral nerves; it is also known as hereditary motor and sensory neuropathy (HMSN). Charcot-Marie-Tooth disease is a group of disorders that affect the peripheral nerves, the nerves running from outside the brain and spine. The peripheral nerves are found outside the … This rare, inherited, slowly progressive neuropathies that came to be known as Charcot-Marie-Tooth (CMT) disorders were described independently in 1886 by Charcot and Marie in France and by Tooth in the UK. It's also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy (PMA). These nerves are responsible for passing on commands from the brain to the muscles (motor nerves) and for passing information to the brain about sensations, such as pain, heat, cold, touch, importantly for balance – where your joints are in space (sensory nerves). Read more about research projects funded by the charity Charcot-Marie-Tooth UK. Defects in many different genes cause different forms of this disease. Treatment for Charcot-Marie-Tooth disease is likely to be orchestrated by a neurologist, but is likely to involve many other hospital departments and healthcare professionals. CMT stands for Charcot-Marie-Tooth disease, named after the three physicians who first described it in 1886: Jean-Martin Charcot, Pierre Marie in France and Howard Henry Tooth in the UK. One day I found an article about Dr. Herrmann’s involvement with a research study for Charcot-Marie-Tooth (CMT) patients and high doses of Vitamin-C. Read More CMT is a group of rare and inherited conditions that damage peripheral nerves and is also known as hereditary motor and sensory neuropathy (HMSN). Onset can occur at any age but is most frequent in the first and second decades of life [1,2]. Charcot-Marie-Tooth Disease is a genetic condition that damages peripheral nerves. Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body. A comprehensive history and physical examination remain the core of ascertainment of and evaluation for cases of CMT. A family history of CMT-like symptoms, combined with signs of nerve damage from an individual’s physical exam, could strongly point to CMT or another hereditary neuropathy. What is CMT? Patients with these other, similar treatments (three in total at this point) have developed otherwise typical chronic inflammatory demyelinating neuropathy (CIDP), an acquired disease that affects many of the same nerve fiber types as CMT. The term “CMT” is regarded as being synonymous with hereditary motor sensory neuropathy (HMSN). 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