WebCharcot-Marie-Tooth disease type 1 (CMT1) is a type of peripheral neuropathy, a condition affecting the transmission of information between the central nervous system (brain and spinal cord) and the rest of the body. ... Cause: This condition is caused by a change in the genetic material (DNA). Organizations: Patient organizations are available ... WebCharcot-Marie-Tooth disease is the most common inherited disorder of the peripheral nervous system with an estimated prevalence of 1 in 1214. CMT1 and CMT2 are equally …

Johns Hopkins CMT Center

WebCharcot–Marie–Tooth disease is caused by genetic mutations that cause defects in neuronal proteins. Nerve signals are conducted by an axon with a myelin sheath … WebCharcot-Marie-Tooth disease or CMT can be inherited in an autosomal dominant, an autosomal recessive, or X-linked manner. These are a few of the ways a disorder or trait can be passed down through a family. With autosomal dominant or recessive inheritance, there is a change (mutation or other alteration) in a gene or genes. the hamilton schedule dc

Charcot-Marie-Tooth disease healthdirect

WebCHARCOT-MARIE-TOOTH DISEASE, TYPE 4J; CMT4J ... NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or … WebHowever, the vast majority of people who have had a genetic cause to their CMT found have had one of five conditions, caused by mutations in four genes: CMT1A ( PMP22 … WebCharcot-Marie-Tooth (CMT) disease is an inherited neurological condition that causes problems with the muscles of your feet, legs, arms and hands. Although there is currently no cure, people with CMT can use a variety of therapies and strategies to help manage their symptoms. CMT disease (sometimes called hereditary motor and sensory neuropathy ... the hamilton school at wheeler