Websummary. Charcot-Marie-Tooth Disease, also known as peroneal muscular atrophy, is a common autosomal dominant hereditary motor sensory neuropathy, caused by abnormal peripheral myelin protein, that … WebFeb 6, 2024 · Patients with Charcot-Marie-Tooth (CMT) disease have a significant family history. This history varies depending on the inheritance and penetrance pattern of the particular disorder (see...
Genetic epidemiology of Charcot-Marie-Tooth disease - PubMed
WebMar 8, 2024 · Overview. Charcot (shahr-KOH)-Marie-Tooth disease is a group of inherited disorders that cause nerve damage. This damage is mostly in the arms and legs … chip shop southam
Charcot Marie Tooth - StatPearls - NCBI Bookshelf
WebDriving Directions to Tulsa, OK including road conditions, live traffic updates, and reviews of local businesses along the way. Charcot-Marie-Tooth disease (CMT) is known as a hereditary motor and sensory neuropathy (HMSN) and is the most common inherited neuromuscular disease with a prevalence of approximately 1 in every 2,500 . CMT involves the degeneration of nerve fibres in the body that results in muscle weakness and … See more CMT is caused by genetic mutations with approximately 1000 mutations in 80 genes that are related to the physical presentation of the disease. The diagnosis and classification of CMT is a very complicated … See more The signs and symptoms of CMT are extremely variable between each different type due the extensive amount of different mutations possible. Symptoms most often begin in adolescence … See more There is currently no cure or drug therapy for CMT. The main treatment options are rehabilitation therapy which will involve both a physiotherapist and an occupational … See more Websummary Charcot-Marie-Tooth Disease, also known as peroneal muscular atrophy, is a common autosomal dominant hereditary motor sensory neuropathy, caused by abnormal peripheral myelin protein, that presents … chip taylor hanger clinic