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

Charcot-Marie-Tooth disease Microchapters

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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

Epidemiology and Demographics

Diagnosis

The diagnosis is established by electromyography examination (which shows that the velocity of nerve impulse conduction is decreased and the time required to charge the nerve is increased) and nerve biopsy. Genetic markers have been identified for some, but not all forms of the disease.

Genetic testing

Genetic testing is available for many of the different types of Charcot-Marie-Tooth. For a listing of test availabilities, see GeneTests.org

External links

References

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