Encephalopathy causes: Difference between revisions
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|bgcolor="Beige"| [[Chromosome 18 Ring ]], [[Pyridoxamine 5-prime-phosphate oxidase deficiency ]], [[Chromosome 9, trisomy 9q ]], [[Chromosome 9q duplication syndrome ]] | |bgcolor="Beige"| [[Chromosome 18 Ring ]], [[Pyridoxamine 5-prime-phosphate oxidase deficiency ]], [[Chromosome 9, trisomy 9q ]], [[Chromosome 9q duplication syndrome ]], [[Bonnemann-Meinecke-Reich syndrome ]], [[Landau–Kleffner syndrome ]], [[Lennox–Gastaut syndrome]], [[Ohtahara syndrome ]], [[West syndrome]], [[Carnitine deficiency syndromes ]], [[Carnitine palmitoyl transferase deficiency ]], [[Carnitine transporter deficiency ]], [[Cytochrome c oxidase deficiency ]], [[MELAS ]], [[NADH CoQ reductase deficiency ]] | ||
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Revision as of 01:18, 24 July 2012
Encephalopathy |
Diagnosis |
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Treatment |
Encephalopathy causes On the Web |
American Roentgen Ray Society Images of Encephalopathy causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2]
Overview
Encephalopathy alters brain function and/or structure.It may be caused by an infectious agent (bacteria, virus, orprion), metabolic or mitochondrial dysfunction, brain tumor or increased intracranial pressure, prolonged exposure to toxins (including solvents, drugs, alcohol, paints, industrial chemicals, and certain metals), radiation, chronic progressive trauma, poor nutrition, or lack of oxygen or blood flow to the brain. It is also known that concomitant use of lithium with other neuroleptics may, in rare cases, cause encephalopathy.