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Article
September 1968

Acute Encephalopathy in Children Associated With Acute Hepatocellular Dysfunction: Reye's Syndrome Revisited

Author Affiliations

Danbury, Conn
From the departments of pediatrics (Dr. Randolph) and pathology (Dr. Gelfman), Danbury Hospital, Danbury, Conn. The authors are also affiliated with the departments of pediatrics and pathology of the Yale University School of Medicine, New Haven, Conn.

Am J Dis Child. 1968;116(3):303-307. doi:10.1001/archpedi.1968.02100020305012
Abstract

SINCE its initial description in Australia in 1963,1 Reye's syndrome has been reported from South Africa,2 Czechoslovakia,3 and the United States.4-6 To date there have been 84 cases reported, with 70 deaths6 and a mortality of 83%. Excepting Reye's original report of 21 patients and Anderson's report the same year, cases have been reported singly or in small clusters, the latter reports suggesting a common etiologic agent. Yet in spite of appropriate viral studies and inquiries into possible access to drugs and poisons, no virus or toxic agent has been consistently identified with this disease.

In 1965, we reported the death of an 8-year-old boy with Reye's syndrome.4 Of epidemiologic interest was the fact that a sibling concurrently developed a similar illness with elevated transaminase values consistent with a mild form of the syndrome. The sibling's sensorium remained clear and he made a spontaneous

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