Charcot-Marie-Tooth disease: Difference between revisions

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'''For patient information, click [[Charcot-Marie-Tooth disease (patient information)|here]]'''
{{Charcot-Marie-Tooth disease}}
{{Charcot-Marie-Tooth disease}}
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==Diagnosis==
==Diagnosis==
[[Charcot-Marie-Tooth disease history and symptoms|History and Symptoms]] | [[Charcot-Marie-Tooth disease physical examination|Physical Examination]] | [[Charcot-Marie-Tooth disease laboratory findings|Laboratory Findings]] | [[Charcot-Marie-Tooth disease other diagnostic studies|Other Diagnostic Studies]]
[[Charcot-Marie-Tooth disease history and symptoms|History and Symptoms]] | [[Charcot-Marie-Tooth disease physical examination|Physical Examination]] | [[Charcot-Marie-Tooth disease laboratory findings|Laboratory Findings]] | [[Charcot-Marie-Tooth disease other diagnostic studies|Other Diagnostic Studies]]
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 marker]]s have been identified for some, but not all forms of the disease.
 
===Genetic testing===
==Treatment==
Genetic testing is available for many of the different types of Charcot-Marie-Tooth.  For a listing of test availabilities, see [http://www.genetests.org GeneTests.org]
 
[[Charcot-Marie-Tooth disease medical therapy|Medical Therapy]] | [[Charcot-Marie-Tooth disease surgery|Surgery]] | [[Charcot-Marie-Tooth disease primary prevention|Primary Prevention]] | [[Charcot-Marie-Tooth disease cost-effectiveness of therapy|Cost-Effectiveness of Therapy]] | [[Charcot-Marie-Tooth disease future or investigational therapies|Future or Investigational Therapies]]


==External links==
==External links==
* {{DMOZ|Health/Conditions_and_Diseases/Neurological_Disorders/Peripheral_Nervous_System/Charcot-Marie-Tooth_Disease/}}
* {{DMOZ|Health/Conditions_and_Diseases/Neurological_Disorders/Peripheral_Nervous_System/Charcot-Marie-Tooth_Disease/}}
==References==
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{{Muscular Dystrophy}}
{{Muscular Dystrophy}}

Latest revision as of 18:52, 22 August 2012

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

For patient information, click here

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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