Charcot-Marie-Tooth disease type 1A (CMT1A) is a type of inherited neurological disorder that affects the peripheral nerves. People with this disease experience weakness and wasting …

Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common form of CMT, accounting for about half of people with CMT. Learn more here.

2023年3月8日 · Charcot-Marie-Tooth disease is also called hereditary motor and sensory neuropathy. Charcot-Marie-Tooth disease results in smaller, weaker muscles. You may also …

CMT Type 1 (CMT1) is defined as an autosomal dominant demyelinating form of Charcot-Marie-Tooth disease. Learn more about CMT1 and subtypes.

2025年1月6日 · Charcot-Marie-Tooth disease (CMT) is a group of genetic conditions that affect the nerves connecting the brain and spinal cord to the rest of the body. CMT is the most …

2024年6月22日 · CMT type 1A, the most common CMT neuropathy, is caused by a 1.5-Mb duplication of chromosome 17p11.2, resulting in trisomy of PMP22. Due to its large size, this …

The CMTA is a nonprofit organization aimed at improving the lives of those impacted by CMT. Learn more and donate to help us create a world without CMT.

CMT1A is the single most common form of Charcot-Marie-Tooth disease. This sub-type of CMT is caused by the duplication of the Peripheral Myelin Protein 22 (PMP22) gene, which leads to …

2025年2月17日 · Charcot-Marie-Tooth disease can be divided into many different subtypes, depending on the specific genetic mutation you are affected by, the moment the first …

Charcot-Marie-Tooth disease type 1A (CMT1A) is a type ofinherited neurological disorder that affects the peripheral nerves. Affected individuals experience weakness and wasting (atrophy) …