Charcot-Marie-Tooth disease type 2 caused by mutation in MFN2 is a rare inherited nerve disease where the long nerves to the feet and hands slowly become weak and thin (degenerate). It mainly affects ...
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2 (often shortened to CMT2A2) is a rare inherited nerve disease where the long “wires” of the peripheral nerves (the axons) slowly become ...
Charcot-Marie-Tooth disease type 2A2 (CMT2A2) is a rare genetic nerve disease that slowly damages the long nerves in the arms and legs. It mainly affects the “axons,” which are the long cable-like ...
Charcot-Marie-Tooth neuropathy type 2A1 (CMT2A1) is a very rare inherited nerve disease. It mainly damages the long nerves that carry signals to and from the feet, legs, hands, and arms. These are ...
Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B is a very rare inherited nerve disease. It belongs to the CMT type 2 group, which mainly damages the long “wires” of the nerves (the ...
Charcot-Marie-Tooth disease neuronal type 2A1 (often shortened to CMT2A1) is a rare, inherited nerve disease that mainly damages the long nerves in the arms and legs. It belongs to the “axonal” forms ...
Autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1 (often shortened to CMT2A1) is a rare, inherited nerve disease that mainly damages the long nerves in the arms and legs, especially the ...
Charcot-Marie-Tooth disease type 2A1 (CMT2A1) is a rare inherited nerve disease that mainly damages the long nerves in the arms and legs. These nerves are called peripheral nerves and they carry ...
Inherited neuronal peroneal muscular atrophy is another name that doctors often use for Charcot–Marie–Tooth disease (CMT), especially the classic “peroneal muscular atrophy” form. It is a genetic ...
Hereditary motor and sensory neuropathy type 2 (HMSN type 2) is a group of inherited nerve diseases where the long “wires” of the nerves (axons) slowly degenerate. These nerves carry signals from the ...
Hereditary motor and sensory neuropathy, Okinawa type, is a very rare inherited nerve disease that damages both the movement nerves (motor) and feeling nerves (sensory) in the body. It mainly affects ...
Hereditary motor and sensory neuropathy Guadalajara neuronal type is a very rare inherited nerve disease that belongs to the Charcot-Marie-Tooth (CMT) family, especially the axonal type called CMT ...
Autosomal dominant axonal Charcot-Marie-Tooth disease is a group of inherited nerve disorders in which the long “wires” of the nerves (axons) slowly become damaged. These nerves carry movement ...
Charcot-Marie-Tooth disease type 2 (CMT2) is a group of inherited nerve diseases in which the long part of the nerve cell (the axon) slowly becomes damaged. This damage affects the peripheral nerves, ...
Charcot-Marie-Tooth neuropathy type 1F/2E (often called NEFL-related CMT or CMT2E/1F) is a rare inherited disease of the peripheral nerves. These nerves carry messages from the brain and spinal cord ...
Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL is a rare inherited nerve disease that mainly affects the peripheral nerves, which are the long nerves that carry signals between the ...
Charcot-Marie-Tooth disease type 1F (CMT1F) is a rare inherited nerve disease that mainly affects the long nerves in the arms and legs. It is part of the big Charcot-Marie-Tooth (CMT) group of ...
Charcot-Marie-Tooth neuropathy type 1E (CMT1E) is a very rare inherited nerve disease. It affects the peripheral nerves, which are the long nerves that carry signals between the brain, spinal cord, ...
Charcot-Marie-Tooth disease–hearing loss syndrome is a rare inherited nerve disorder in which a person has both Charcot-Marie-Tooth (CMT) disease and sensorineural hearing loss. CMT is a group of ...
Charcot-Marie-Tooth disease–deafness syndrome is a very rare inherited nerve disease in which a person has both Charcot-Marie-Tooth (CMT) neuropathy and significant hearing loss, often from childhood ...
