Charcot-Marie-Tooth disease/Definition: Difference between revisions

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(New page: <noinclude>{{Subpages}}</noinclude> A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss...)
 
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A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy ( HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., ''Principles of Neurology'', 6th ed, p1343)
Part of a family of hereditary motor and sensory neuropathies transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. <noinclude>{{DefMeSH}}</noinclude>

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A definition or brief description of Charcot-Marie-Tooth disease.

Part of a family of hereditary motor and sensory neuropathies transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life.

This definition is at least in part based on: Anonymous (2024), Charcot-Marie-Tooth disease (English). Medical Subject Headings. U.S. National Library of Medicine.

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