Charcot–Marie–Tooth disease
(Redirected from 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
- Human male karyotpe high resolution - Chromosome 17 cropped.png
Pair of human chromosome 17 after G-banding. One is from mother, one is from father.
- Denervation atrophy - atp94 - intermed mag.jpg
Denervation atrophy of type II muscle fibers
- Charcot Marie Tooth CMT.jpg