Charcot-Marie-Tooth disease: Difference between revisions
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{{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]] | |||
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. | 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=== | |||
==Genetic testing== | |||
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] | 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] | ||
Revision as of 17:56, 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 |
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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 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