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  2. Charcot-Marie-Tooth disease

Charcot-Marie-Tooth disease

  • CMT
  • Hereditary motor and sensory neuropathies
  • Peroneal muscular atrophy

Nature

Charcot-Marie-Tooth disease (CMT)is actually a broad term used to describe a group of genetic disorders that affects the peripheral nerves, which carry motor (relating to movement) and sensory (relating to sensation) signals between the brain and spinal cord and the rest of the body. CMT most frequently affects the lower legs, feet and hands, resulting in weakness and atrophy, or loss of muscle bulk, as well as causing a mild degree of loss of sensation. However, the motor problems are much more significant than the sensory problems, which are usually minor.

Incidence

About one in 2,500 people has a form of CMT. Overall, it affects about 100,000 to 125,000 people in the USA alone, making it one of the most common hereditary disorders.

Broader

Value

Disease
Yet to rate

Web link

SDG

Sustainable Development Goal #3: Good Health and Well-being

Metadata

Database
World problems
Type
(G) Very specific problems
Subject
  • Biosciences » Genetics
  • Industry » Machinery
  • Medicine » Locomotive, integumentary system
  • Medicine » Muscular system » Muscular system
  • Medicine » Nervous system » Nervous system
  • Medicine » Pathology
  • Medicine » Teeth, mouth
  • Psychology » Sensory
  • Content quality
    Presentable
     Presentable
    Language
    English
    Last update
    Nov 2, 2022