Charcot–Marie–Tooth disease

Charcot–Marie–Tooth disease (CMT), also known as Charcot–Marie–Tooth neuropathy, hereditary motor and sensory neuropathy (HMSN) and peroneal muscular atrophy (PMA) — is a genetically and clinically heterogeneous group of inherited disorders of the peripheral nervous system characterised by progressive loss of muscle tissue and touch sensation across various parts of the body.

Charcot–Marie–Tooth Disease Media

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  Pair of human chromosome 17 after G-banding. One is from mother, one is from father.

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  Denervation atrophy of type II muscle fibers

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  Ankle-foot orthosis