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(redirected from Charcot-Marie-Tooth disease)

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According to a study published in the Lancet Journal, Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary peripheral neuropathy that affects roughly one in 5000 births.
Among the categories covered are: spinal muscular atrophies, poliomyelitis, Charcot-Marie-Tooth disease and related disorders, vasculitic neuropathies, neuropathies associated with infections, muscular dystrophies, congenital myopathies, myotonic dystrophies, and toxic myopathies, among others.
The genetic data indicate that several genes may be causing this disorder, but one large gene is a particularily good candidate gene because some mutations in this gene cause Charcot-Marie-Tooth disease, a sensory neuropathy.
 
 
 
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