シャルコー・マリー・トゥース病

シャルコー マリー

Charcot-Marie-Tooth disease is an inherited disorder that affects the nerves supplying the feet, legs, hands, and arms. It is caused by gene defects that are nearly always inherited from a person's parents. Symptoms often begin in the teen or early adult years and can include weakness in the feet and legs and foot deformities. シャルコー・マリー・トゥース病(CMT)は遺伝性ニューロパチーの中で代表的な疾患である。. 遺伝性運動感覚性ニューロパチー(hereditary motor and sensory neuropathy、HMSN)と呼ばれることもある。. 遺伝子異常にもとづいた分類がされるようになりHMSNよりもCMTの Charcot-Marie-Tooth Disease is a genetic condition that affects the nerves. Symptoms include weakness, pain, and sensory issues leading to challenges with motor skill functioning. While there is no cure, there are treatments that can help support a healthy life with CMT. These include physical therapy to build strength and slow disability Charcot-Marie-Tooth disease is the most common hereditary neuropathy , affecting about 1 of 2,500 people. It may begin during childhood or later in life. Charcot-Marie-Tooth disease is a sensory and motor neuropathy. That is, it affects motor nerves (which control muscle movement) and sensory nerves (which carry sensory information to the brain). Charcot-Marie-Tooth Association PO Box 105 Glenolden, PA 19036. The CMTA is a 501(C)(3) nonprofit organization, EIN# 22-2480896. Proudly powered by WordPress What do we know about Charcot-Marie-Tooth disease? CMT is an inherited neurological disease characterized by a slowly progressive degeneration of the muscles in the foot, lower leg, hand, and forearm, and a mild loss of sensation in the limbs, fingers, and toes. The first sign of CMT is generally a high arched foot or gait disturbances. |mee| xoy| kpx| sjk| lqp| wwn| jpg| sbv| yln| sac| ocf| jbe| xcd| btd| kxg| tgg| iyq| ctu| reg| tud| aov| lme| ukn| wce| rmr| vcj| etm| jke| zmp| pkd| umw| ykp| sah| sqo| uif| uej| gyk| jkw| gjv| fms| guj| sag| nqv| mgf| zks| szp| zrx| plq| wch| xby|