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Charcot-Marie-Tooth disease type 1 (medical condition): A slow-progressing muscle disease characterized by muscle weakness and wasting that starts in the hands and feet. Very few patients become wheelchair dependent and life span is not affected. The disorder is inherited in an dominant pattern an involves demyelination of the nerves.
See also:
Charcot-Marie-Tooth disease, type 1:
»Introduction: Charcot-Marie-Tooth disease, type 1
»Symptoms of Charcot-Marie-Tooth disease, type 1
Charcot-Marie-Tooth disease type 1: 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)
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Charcot-Marie-Tooth disease type 1:
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Charcot-Marie-Tooth disease type 1 as a "rare disease".
Source - Orphanet
Charcot-Marie-Tooth disease type 1 (medical condition): See Charcot-Marie-Tooth disease, type 1 (disease information).
»Introduction: Charcot-Marie-Tooth disease, type 1
»Symptoms of Charcot-Marie-Tooth disease, type 1
Source: Diseases Database
Source: Diseases Database
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