Charcot-Marie-Tooth disease, axonal, type 2GG (often shortened to CMT2GG) is a very rare, inherited nerve disease that mainly affects the long nerves in the legs and sometimes the hands. It is an ...
Charcot-Marie-Tooth neuropathy type 2D (CMT2D) is a rare inherited nerve disease that mainly affects the small nerves to the hands and feet. It is an “axonal” neuropathy, which means the long ...
ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2 is a rare inherited nerve disease. It happens when there is a harmful change (mutation) in a gene called ATP1A1. This gene gives ...
ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2 (often called CMT2DD) is a very rare inherited nerve disease. It mainly damages the “wires” (axons) of the peripheral nerves, ...
Charcot-Marie-Tooth disease, axonal, type 2DD (CMT2DD) is a rare inherited nerve disease. It mainly damages the long nerves that carry signals to and from the feet, legs, hands, and arms. These ...
Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres is a very rare inherited nerve disease. It affects the long nerves that carry ...
Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers is a very rare inherited nerve disease. Doctors also call it a special type ...
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome is a very rare inherited nerve disease. It affects the nerves that control movement and the nerves that carry sound from the ...
Rosenberg-Chutorian syndrome is an extremely rare genetic nerve disease. It mainly affects three parts of the body at the same time: the ears (hearing), the eyes (optic nerve), and the peripheral ...
PRPS1-related Charcot-Marie-Tooth neuropathy X type 5 (often called CMTX5) is a very rare, inherited nerve disease. It mainly affects the long nerves of the arms and legs, the hearing nerve, and the ...
Distal neurogenic amyotrophy is a general medical phrase that means nerve-related muscle wasting that mainly affects the far (distal) parts of the arms and/or legs, such as the hands, forearms, feet, ...
Familial opticoacoustic nerve degeneration and polyneuropathy is a very rare inherited nerve disease in which three main problems happen together: damage to the optic nerves (the nerves for vision), ...
Charcot-Marie-Tooth neuropathy X-linked recessive 5 (often shortened to CMTX5) is a very rare inherited nerve disease that mainly damages the long nerves in the arms and legs and also affects hearing ...
Charcot-Marie-Tooth neuropathy X type 5 (often shortened to CMTX5) is a very rare inherited nerve disease. It mainly affects the peripheral nerves, which are the long nerves that carry signals ...
X-linked recessive diseases are a group of genetic (inherited) diseases caused by a harmful change (variant) in a gene that sits on the X chromosome. Because most boys and men have one X chromosome, ...
Charcot-Marie-Tooth disease X-linked recessive 5 (often called CMTX5) is a very rare, inherited nerve disease. It mainly damages the long nerves to the feet, legs, hands, and eyes and the hearing ...
Cowchock syndrome is a very rare genetic nerve disease. It mainly affects the long nerves in the arms and legs, the hearing nerve, and sometimes the brain. It causes weakness and wasting of muscles, ...
Charcot-Marie-Tooth neuropathy X type 4 (often written as CMTX4) is a very rare, inherited nerve disease. It mainly damages the long nerves that control movement and feeling in the legs and arms ...
Charcot-Marie-Tooth disease, X-linked recessive, 4, with or without cerebellar ataxia is a very rare inherited nerve disease that mainly affects the long nerves in the arms and legs and sometimes ...
Charcot–Marie–Tooth disease with deafness and intellectual disability is a very rare genetic nerve disease. It affects the long nerves that control movement and carry messages about sound and ...
