Charcot-Marie-Tooth disease

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Charcot-Marie-Tooth disease
The foot of a person with Charcot-Marie-Tooth. The lack of muscle, a high arch, and hammer toes are signs of the genetic disease.
ICD-10 G60.0
ICD-9 356.1
DiseasesDB 5815 Template:DiseasesDB2
MedlinePlus 000727
MeSH D002607

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Hereditary motor and sensory neuropathy; peroneal muscular atrophy

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Charcot-Marie-Tooth disease from other Diseases

Epidemiology and Demographics

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies

Treatment

Medical Therapy | Surgery | Primary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

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Template:Muscular Dystrophy Template:PNS diseases of the nervous system


ca:Malaltia de Charcot-Marie-Tooth de:Morbus Charcot-Marie-Tooth it:Malattia di Charcot-Marie-Tooth nl:Hereditaire Motorische en Sensorische Neuropathieën no:Charcot-Marie-Tooths sykdom sv:Charcot-Marie-Tooths sjukdom

Template:WS