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Charcot-Marie-Tooth disease (CMT) is a group of genetic nerve disorders. It is named after the three doctors who first identified it. In the United States, CMT affects about 1 in 2,500 people.
CMT affects your
- Charcot-Marie-Tooth Disease (National Library of Medicine)Charcot-Marie-Tooth disease (CMT) is a group of genetic nerve disorders. It is named after the three doctors who first identified it. In the United States, CMT ...
- ... Philadelphia, PA: Elsevier; 2022:chap 106. Sarnat HB. Hereditary motor-sensory neuropathies. In: Kliegman RM, St. Geme JW, Blum NJ, ...
- ... features, Andermann syndrome is sometimes referred to as hereditary motor and sensory neuropathy with agenesis of the corpus callosum (HMSN/ACC). ... Agenesis of corpus callosum with polyneuropathy Charlevoix disease Hereditary motor and sensory neuropathy with agenesis of the corpus callosum HMSN/ACC ...
- ... Compression neuropathy Entrapment neuropathy Familial pressure sensitive neuropathy Hereditary motor and sensory neuropathy Hereditary pressure sensitive neuropathy HNPP Inherited tendency to ...
- ... AND DEAFNESS KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS CHARCOT-MARIE-TOOTH ...
- The TRPV4 gene provides instructions for making a protein that acts as a calcium channel. This channel, which transports positively charged atoms of calcium ( ...
- ... Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol. ... on PubMed Gauvreau C, Brisson JD, Dupre N. Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum. 2006 Feb ...
- Peripheral Nerve Disorders/Specifics ... Peripheral Nerve Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health
- ... include impaired vision. (This variant is also called hereditary motor and sensory neuropathy VI.) Vision loss is caused by the breakdown ... mitochondrial assembly regulatory factor Tests of MFN2 PubMed NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A MITOFUSIN 2; ...
- ... Adult Refsum disease ARD Classic Refsum disease CRD Hereditary motor and sensory neuropathy type IV Heredopathia atactica polyneuritiformis HMSN IV HMSN ...