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

What is Charcot-Marie-Tooth disease type 1 (CMT1)? CMT type 1 is the most common subtype of CMT, accounting for roughly two-thirds of all cases. CMT1 is inherited in an autosomal dominant pattern.

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 common inherited neuropathy. Neuropathy describes a nerve condition that causes pain, swelling, or …

Charcot-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.

CMT1 is a form of CMT that is inherited with autosomal dominance (its inheritance pattern). This means the disease occurs with at least one copy of the disease-causing gene, and affected individuals usually also have one normal copy of the gene …

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 (atrophy) of the muscles of the lower legs beginning in adolescence; later they can also have hand weakness and sensory loss.

2023年3月8日 · 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 (peripheral nerves). Charcot-Marie-Tooth disease is also called hereditary motor and sensory neuropathy. Charcot-Marie-Tooth disease results in smaller, weaker muscles.

2022年11月29日 · Charcot-Marie-Tooth disease (CMT) is the name for a group of conditions that all affect how your peripheral nerves (the nerves outside of your brain and spinal cord) work. This condition usually affects muscle control and how you feel your feet and hands. It …

Charcot-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. The condition is usually slowly progressive.

CMT Type 1 (CMT1) is defined as an autosomal dominant (see inheritance.) demyelinating form of CMT. CMT1 accounts for about 55 percent of all cases of CMT. Learn more about CMT Type 1 and subtypes. What is Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)? HNPP is inherited in an autosomal dominant pattern.