Charcot-Marie-Tooth disease: Difference between revisions
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MeshID = D002607 | | MeshID = D002607 | | ||
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'''For patient information, click [[Charcot-Marie-Tooth disease (patient information)|here]]''' | |||
{{Charcot-Marie-Tooth disease}} | {{Charcot-Marie-Tooth disease}} | ||
{{CMG}} | {{CMG}} | ||
{{SK}} Hereditary motor and sensory neuropathy; peroneal muscular atrophy | {{SK}} Hereditary motor and sensory neuropathy; peroneal muscular atrophy | ||
==[[Charcot-Marie-Tooth disease overview|Overview]]== | ==[[Charcot-Marie-Tooth disease overview|Overview]]== | ||
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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]] | ||
==Treatment== | |||
[[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/}} | ||
{{Muscular Dystrophy}} | {{Muscular Dystrophy}} | ||
Latest revision as of 18:52, 22 August 2012
| Charcot-Marie-Tooth disease | |
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| 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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Charcot-Marie-Tooth disease Microchapters |
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Differentiating Charcot-Marie-Tooth disease from other Diseases |
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Diagnosis |
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Treatment |
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Charcot-Marie-Tooth disease On the Web |
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American Roentgen Ray Society Images of Charcot-Marie-Tooth disease |
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Directions to Hospitals Treating Charcot-Marie-Tooth disease |
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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