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      Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders.

      Archives of neurology

      Animals, Genetic Predisposition to Disease, Homocystinuria, complications, genetics, Humans, Metabolism, Inborn Errors, Models, Biological, Stroke, etiology, Urea Cycle Disorders, Inborn

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          Abstract

          Several inherited metabolic disorders have been associated with stroke particularly in newborns, children, and young adults. In part 1, we discussed the genetics, stroke pathophysiology, clinical presentation, diagnosis, and treatment of Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. In part 2, we overview homocystinuria, organic acidurias, and urea cycle disorders.

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          Journal
          20142522
          10.1001/archneurol.2009.333

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