Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant

Common Name(s)

Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant

Hereditary motor and sensory neuropathies (HMSN) are a heterogeneous group of peripheral nervous system disorders affecting motor and sensory function. HMSN I, also known as Charcot-Marie-Tooth (CMT) disease, or peroneal muscular atrophy, type 1, is a demyelinating neuropathy (see CMT1B; {118200}) and HMSN II, also known as CMT type 2, is an axonal neuropathy (see CMT2A1; {118210}). See also HMSN III ({145900}) and HMSN IV ({266500}). For an autosomal recessive disorder with similarities to HMSN V, see {607731}.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant" for support, advocacy or research.

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Scientific Literature

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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