Charcot-Marie-Tooth disease axonal type 2V

Charcot-Marie-Tooth disease axonal type 2V is a form of Charcot-Marie-Tooth disease that is caused by a mutation in the NAGLU gene. This condition is part of a group of inherited disorders that affect the peripheral nerves, which are responsible for movement and sensation in the arms and legs. The genetic basis of this condition clearly distinguishes it from other forms of Charcot-Marie-Tooth disease. It has been identified through gene studies and is also known by other names, including CMT2V and Charcot-Marie-Tooth neuropathy type 2V. Information about the range and severity of symptoms may vary, and further details are still being explored by researchers.

Information about symptoms is currently limited for this condition.

This condition is caused by a mutation in the NAGLU gene. Genetic mutations in this gene are the underlying cause of the changes seen in people with this form of Charcot-Marie-Tooth disease.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.