Charcot-Marie-Tooth disease
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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Charcot-Marie-Tooth disease Microchapters |
Differentiating Charcot-Marie-Tooth disease from other Diseases |
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Charcot-Marie-Tooth disease On the Web |
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Risk calculators and risk factors for Charcot-Marie-Tooth disease |
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
External links
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