Axonal motor sensory neuropathy with deafness and intellectual disability is a very rare inherited nerve disease. It mainly affects the long nerves that carry signals from the brain and spinal cord ...
Charcot-Marie-Tooth disease X-linked recessive 4 (often written as CMTX4) is a very rare inherited nerve disease. It mainly damages the long nerves that carry signals to and from the arms and legs. ...
Charcot-Marie-Tooth neuropathy X-linked recessive 2 (often called CMTX2) is a very rare inherited nerve disease that mainly affects the long nerves going to the feet, legs, hands, and arms. These ...
Charcot-Marie-Tooth neuropathy X type 2 (often written as CMTX2) is a very rare, inherited nerve disease. It affects the peripheral nerves. These are the long nerves that carry movement and feeling ...
Charcot-Marie-Tooth disease X-linked recessive 2 (often shortened to CMTX2) is a very rare inherited nerve disease. It mainly damages the long nerves that go from the spinal cord to the feet and ...
Charcot-Marie-Tooth neuropathy X-linked dominant 6 (often called CMTX6) is a very rare, inherited nerve disease that mainly affects the long nerves in the legs and feet. It causes slow and steady ...
Charcot-Marie-Tooth disease X-linked dominant 6 (often shortened to CMTX6) is a very rare, inherited nerve disease that mainly affects the long nerves to the feet, legs, hands, and arms. It belongs ...
Charcot-Marie-Tooth neuropathy X-linked dominant 1 (often called CMTX1) is a rare inherited nerve disease that mainly affects the “long wires” of the body, called peripheral nerves. These nerves ...
Charcot-Marie-Tooth disease X-linked dominant type 1 (often called CMTX1 or CMT1X) is a rare inherited nerve disease. It mainly damages the peripheral nerves, which carry messages to and from the ...
Charcot-Marie-Tooth disease type X caused by mutation in GJB1 (often called CMTX1) is a rare, inherited nerve disease. It mainly damages the “peripheral nerves.” These are the long nerves that carry ...
Charcot-Marie-Tooth disease X-linked dominant 1 (often called CMTX1) is a genetic nerve disease. It mainly affects the peripheral nerves, which are the long nerves that carry signals from the spinal ...
X-linked hereditary motor and sensory neuropathy is a long-term nerve disease that mainly damages the nerves in the legs, feet, hands, and arms. These nerves carry signals from the brain to the ...
Charcot-Marie-Tooth disease type X (often written as CMTX or CMTX1) is a genetic nerve disease. It mainly affects the peripheral nerves, which are the nerves outside the brain and spinal cord. These ...
Hereditary motor and sensory neuropathy with pyramidal features is a very rare nerve disease that runs in families. It affects the long nerves that move the muscles (motor nerves) and the nerves that ...
Hereditary motor and sensory neuropathy type V (HMSN V) is a very rare inherited nerve disease. It affects both the motor nerves (that move muscles) and the sensory nerves (that feel touch, pain, and ...
Hereditary motor and sensory neuropathy type 5 (HMSN type 5) is a very rare form of Charcot–Marie–Tooth (CMT) disease. Doctors also call it “Charcot–Marie–Tooth disease type 5,” “hereditary motor and ...
Charcot-Marie-Tooth (CMT) disease–pyramidal features syndrome is a rare, inherited nerve disease in which a person has both signs of CMT (damage to the long peripheral nerves in the arms and legs) ...
Charcot-Marie-Tooth disease type 5 (CMT type 5) is a rare inherited nerve disease that mainly damages the long nerves to the feet, legs, hands, and arms and also affects the “pyramidal tracts,” which ...
Cytochrome c oxidase assembly factor–related Charcot-Marie-Tooth disease type 4 is a very rare inherited nerve disease where the long nerves in the arms and legs slowly stop working well. It is ...
Surf1-related severe demyelinating Charcot-Marie-Tooth (CMT) disease is a very rare inherited nerve disease. It mainly damages the long nerves that go from the spinal cord to the feet and hands. ...
