Encephalopathy classification: Difference between revisions
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There are many types of encephalopathy. | There are many types of encephalopathy. | ||
* [[Hepatic encephalopathy]] - Arising from advanced cirrhosis of the liver | * [[Hepatic encephalopathy]] - Arising from advanced cirrhosis of the liver | ||
* [[Hypoxic encephalopathy]] - Permanent or transitory encephalopathy arising from severely reduced oxygen delivery to the brain | * [[Hypoxic encephalopathy]] - Permanent or transitory encephalopathy arising from severely reduced oxygen delivery to the brain | ||
* [[Wernicke's encephalopathy]] - Arising from thiamine deficiency, usually in the setting of alcoholism | * [[Wernicke's encephalopathy]] - Arising from thiamine deficiency, usually in the setting of alcoholism | ||
* [[Hashimoto's encephalopathy]] - Arising from an auto-immune disorder | * [[Hashimoto's encephalopathy]] - Arising from an auto-immune disorder | ||
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* [[Metabolic encephalopathy| | * [[Metabolic encephalopathy| | ||
Toxic Metabolic encephalopathy]] - A catch-all for brain dysfunction caused by infection, organ failure, or intoxication. | Toxic Metabolic encephalopathy]] - A catch-all for brain dysfunction caused by infection, organ failure, or intoxication. | ||
* [[Uremic encephalopathy]] - Arising from high levels of toxins normally cleared by the kidneys -- rare where dialysis is readily available | |||
* [[MELAS|Mitochondrial encephalopathy]] - Metabolic disorder caused by dysfunction of mitochondrial DNA. Can affect many body systems, particularly the brain and nervous system. | |||
* [[Glycine encephalopathy]] - A pediatric metabolic disorder | |||
* [[Static encephalopathy]] - Unchanging, or permanent, brain damage | |||
* [[Transmissible spongiform encephalopathy]] - A collection of diseases all caused by prions, and characterized by "spongy" brain tissue (riddled with holes), impaired locomotion or coordination, and a high fatality rate. Includes [[bovine spongiform encephalopathy]] (mad cow disease), [[scrapie]], and [[Kuru (disease)|kuru]] among others. | * [[Transmissible spongiform encephalopathy]] - A collection of diseases all caused by prions, and characterized by "spongy" brain tissue (riddled with holes), impaired locomotion or coordination, and a high fatality rate. Includes [[bovine spongiform encephalopathy]] (mad cow disease), [[scrapie]], and [[Kuru (disease)|kuru]] among others. | ||
==References== | ==References== | ||
Revision as of 20:23, 19 July 2012
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Encephalopathy |
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Treatment |
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Encephalopathy classification On the Web |
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American Roentgen Ray Society Images of Encephalopathy classification |
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Risk calculators and risk factors for Encephalopathy classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]
Overview
There is no specific classification scheme,but different kinds of encephalopahties are termed basing upon their pathophysiology.
Classification
There are many types of encephalopathy.
- Hepatic encephalopathy - Arising from advanced cirrhosis of the liver
- Hypoxic encephalopathy - Permanent or transitory encephalopathy arising from severely reduced oxygen delivery to the brain
- Wernicke's encephalopathy - Arising from thiamine deficiency, usually in the setting of alcoholism
- Hashimoto's encephalopathy - Arising from an auto-immune disorder
- Hypertensive encephalopathy - Arising from acutely increased blood pressure
- Toxic Metabolic encephalopathy - A catch-all for brain dysfunction caused by infection, organ failure, or intoxication.
- Uremic encephalopathy - Arising from high levels of toxins normally cleared by the kidneys -- rare where dialysis is readily available
- Mitochondrial encephalopathy - Metabolic disorder caused by dysfunction of mitochondrial DNA. Can affect many body systems, particularly the brain and nervous system.
- Glycine encephalopathy - A pediatric metabolic disorder
- Static encephalopathy - Unchanging, or permanent, brain damage
- Transmissible spongiform encephalopathy - A collection of diseases all caused by prions, and characterized by "spongy" brain tissue (riddled with holes), impaired locomotion or coordination, and a high fatality rate. Includes bovine spongiform encephalopathy (mad cow disease), scrapie, and kuru among others.