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Up to: Hereditary peripheral neuropathy
Charcot-Marie-Tooth disease
An inherited degenerative disorder involving the peripheral nerves. It is caused by mutations in the genes that are responsible for the production of proteins necessary for the function and structure of the peripheral nerves. It is characterized by muscle atrophy and weakness in the feet, legs, hands, and arms and loss of sensation in the limbs.
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Charcot-Marie-Tooth disease type 1 4 trials · 40 incl. sub-types Sub-types →
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Charcot-Marie-Tooth disease type 2 3 trials · 9 incl. sub-types Sub-types →
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Charcot-Marie-Tooth disease type 4 0 trials · 5 incl. sub-types Sub-types →
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Intermediate Charcot-Marie-Tooth disease 0 trials · 3 incl. sub-types Sub-types →
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Charcot-Marie-Tooth disease type X 1 trial · 2 incl. sub-types Sub-types →
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Charcot-Marie-Tooth disease type 3 0 trials