Charcot–Marie–Tooth disease classifications
Charcot–Marie–Tooth disease classifications is a system used to categorize the various types of Charcot–Marie–Tooth disease (CMT), a group of inherited disorders that affect the peripheral nerves. The classification system is based on the genetic cause of the disease, the specific nerves affected, and the pattern of inheritance.
Types of Charcot–Marie–Tooth disease[edit | edit source]
There are several types of CMT, each with its own unique characteristics and genetic causes. These include:
- CMT Type 1: This is the most common type of CMT. It is caused by mutations in the PMP22, MPZ, or EGR2 genes and is characterized by demyelination of the peripheral nerves.
- CMT Type 2: This type of CMT is caused by mutations in a variety of genes and is characterized by axonal degeneration.
- CMT Type 3: Also known as Dejerine-Sottas disease, this severe form of CMT is caused by mutations in the PMP22, MPZ, or EGR2 genes.
- CMT Type 4: This type of CMT is characterized by severe demyelination and is caused by mutations in a variety of genes.
- CMT Type X: This type of CMT is caused by mutations in the GJB1 gene and is characterized by both demyelination and axonal degeneration.
Inheritance Patterns[edit | edit source]
CMT can be inherited in several ways, including:
- Autosomal dominant: This is the most common pattern of inheritance for CMT. It means that an affected person has a 50% chance of passing the disease to each of their children.
- Autosomal recessive: This pattern of inheritance requires both parents to carry a copy of the mutated gene. The risk of passing the disease to their children is 25%.
- X-linked: This pattern of inheritance means that the disease is caused by a mutation on the X chromosome. Males are more severely affected than females.
Diagnosis and Treatment[edit | edit source]
Diagnosis of CMT is based on clinical symptoms, family history, and genetic testing. Treatment is supportive and may include physical therapy, occupational therapy, and assistive devices.
See Also[edit | edit source]
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