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Synonyms

Reye’s syndrome

Definition and Characteristics

Reye syndrome (RS) is a severe pediatric disorder characterized by an acute noninflammatory encephalopathy and fatty degeneration of the liver but it is not a clinical entity [1,2]. RS was first described in 1963 by Reye and colleagues. The illness is typically biphasic, with an apparent near-recovery from a viral type prodromal illness followed after a few days by persistent or recurrent vomiting, personality changes such as irritability, disorientation or confusion, delirium, convulsions, and loss of consciousness. The condition is associated with viral infections (varicella, influenza), with the exposure to toxins and drugs such as aspirin during a viral illness [3,4], and most importantly with underlying inherited metabolic disorders [5].

Prevalence

Peak ages are between 5 and 14 years. The syndrome is rare in early infancy and adulthood. On the basis of the CDC (Center for Disease Control and Prevention), data from the USA,...

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References

  1. Autret-Leca E, Jonville-Bera AP, Llau ME, Bavoux F, Saudubray JM, Laugier J, Devictor D, Barbier P, (2001) Incidence of Reye’s syndrome in France: a hospital-based survey. J Clin Epidemiol 54:857–862 all the French Departments of Paediatrics

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  2. Belay ED, Bresee JS, Holman RC, Khan AS, Shahriari A, Schonberger LB (1999) Reye’s syndrome in the United States from 1981 through 1997. N Engl J Med 340:1377–1382

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  3. Casteels-Van Daele M, Van Geet C, Wouters C, Eggermont E (2000) Reye syndrome revisited: a descriptive term covering a group of heterogeneous disorders. Eur J Pediatr 159:641–648

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  4. Glasgow JF, Middleton B (2001) Reye syndrome-insights on causation and prognosis. Arch Dis Child 85:351–353

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  5. Orlowski JP (1999) Whatever happened to Reye’s syndrome? Did it ever really exist? Crit Care Med 27:1582–1587

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© 2009 Springer-Verlag GmbH Berlin Heidelberg

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Häberle, J., Nuoffer, JM. (2009). Reye Syndrome. In: Lang, F. (eds) Encyclopedia of Molecular Mechanisms of Disease. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-29676-8_1559

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