Charcot-Marie-Tooth disease and deafness (also called CMT1E when caused by some PMP22 gene variants) is a rare inherited nerve disease in which the protective covering of the peripheral nerves ...
Autosomal dominant Charcot-Marie-Tooth neuropathy and deafness is a rare inherited nerve disease. In this condition, the long nerves to the feet and hands become damaged, and the hearing nerve or ...
Charcot-Marie-Tooth disease type 1E (CMT1E) is a rare inherited nerve disease. It mainly harms the peripheral nerves, which are the long nerves that carry signals between the brain/spinal cord and ...
Hereditary motor and sensory neuropathy 1D (HMSN 1D) is a rare, inherited nerve disease. It is the same condition as Charcot-Marie-Tooth disease type 1D (CMT1D). In this disease, the long nerves that ...
Charcot-Marie-Tooth neuropathy type 1D (CMT1D) is a rare, inherited nerve disease that mainly damages the long nerves going to the feet, legs, hands, and arms. It is a “demyelinating” neuropathy, ...
Charcot-Marie-Tooth disease type 1 caused by mutation in the EGR2 gene is a rare, inherited nerve disease that mainly affects the nerves of the arms and legs. Doctors call this group of diseases ...
Charcot-Marie-Tooth disease type 1D (CMT1D) is a rare, inherited nerve disease. It mainly affects the “peripheral nerves”. These are the long nerves that carry signals between your brain, spinal ...
Charcot-Marie-Tooth slow nerve conduction type C is a rare inherited nerve disease that mainly affects the long nerves in the arms and legs. It belongs to the group called Charcot-Marie-Tooth disease ...
Charcot-Marie-Tooth neuropathy type 1C (CMT1C) is a rare, inherited nerve disease. It mainly damages the peripheral nerves, which are the long nerves that carry signals between the spinal cord and ...
Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF is usually called Charcot-Marie-Tooth disease type 1C (CMT1C). It is a rare, inherited nerve disease. It mainly damages the long nerves ...
Charcot-Marie-Tooth disease type 1C (CMT1C) is a rare, inherited nerve disease. It mainly affects the long nerves that control movement and feeling in the feet, legs, hands, and arms. In CMT1C, a ...
Hereditary motor and sensory neuropathy IB (HMSN IB) is another name for Charcot–Marie–Tooth disease type 1B (CMT1B). It is a rare, inherited nerve disease that slowly damages the long nerves in the ...
Hereditary motor and sensory neuropathy (HMSN) is a group of genetic nerve diseases where the nerves that control movement and feeling in the arms and legs slowly stop working properly. These nerves ...
Charcot-Marie-Tooth neuropathy type 1B (CMT1B) is a rare, inherited nerve disease that mainly affects the peripheral nerves in the arms and legs. These nerves normally carry signals for movement and ...
Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ is a long-lasting, inherited nerve disease that mainly damages the nerves in the arms and legs. It is a demyelinating neuropathy, which ...
Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy is a hereditary nerve disease in which the outer covering of the nerves (myelin) is damaged, so nerve signals travel more slowly ...
Autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B (often shortened to CMT1B with focally folded myelin) is a rare inherited nerve disease that mainly affects ...
Charcot-Marie-Tooth disease type 1B (CMT1B) is a rare inherited nerve disease that mainly affects the nerves in the legs, feet, hands, and arms. These nerves are called peripheral nerves. They carry ...
Hereditary motor and sensory neuropathy type 1A (HMSN 1A) is a genetic nerve disease that slowly damages the long nerves in the arms and legs. It mainly affects the “motor” nerves that move muscles ...
Charcot-Marie-Tooth neuropathy type 1A (CMT1A) is an inherited nerve disease that mainly affects the nerves in the arms and legs. These nerves are called peripheral nerves. In CMT1A, the outer ...
