CARNITINE METABOLISM IN RECURRENT REYE SYNDROME DUE TO DEFECTIVE ACETYL-CoA DISPOSAL
نویسندگان
چکیده
منابع مشابه
Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy.
Carnitine deficiency syndrome is a rare and potentially fatal but treatable metabolic disorder. I present a 6-year-old girl with primary systemic carnitine deficiency (SCD) proved by very low plasma carnitine level. Her major clinical features included neonatal metabolic acidosis, epilepsy, recurrent infections, acute encephalopathy, and dilated cardiomyopathy with heart failure before 4 years ...
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This year in the United States there has been considerable controversy about circumstantial evidence linking salicylates to the pathogenesis of Reye syndrome and, in particular, whether that evidence is sufficiently strong to justify action. After careful review both the Federal government and the American Academy of Pediatrics have warned physicians and parents of the possible risk of Reye syn...
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Recent research has clarified many of the clinical applications of L-Carnitine and its related compounds, leading into new areas of potential use. Promising therapeutic applications of an ester form of carnitine, acetyl-L-Carnitine (ALC) are derived from observations that this compound readily crosses the bloodbrain barrier and improves neuronal energetics and repair mechanisms while modifying ...
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ژورنال
عنوان ژورنال: Pediatric Research
سال: 1984
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-198404001-01216