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James Y. Massey, MD; F. Hampton Roy, MD; John H. Bornhofen, MD

Arch Ophthalmol. 1974;91(6):441-444.

Abstract
Reye syndrome is a childhood encephalopathy associated with fatty metamorphosis of the viscera of unknown etiology. The eye findings include dilated pupils that react sluggishly to light or not at all, cortical blindness, and papilledema. Treatment is supportive and 20% to 50% of patients recover completely in three to seven days.

Author Affiliations
Little Rock, Ark

From the departments of ophthalmology, University of Arkansas Medical Center, Veterans Administration Hospital, Arkansas Children's Hospital (Drs. Massey and Roy); and the departments of pediatrics, University of Arkansas Medical Center and Arkansas Children's Hospital, Little Rock (Dr. Bornhofen).

Footnotes
Submitted for publication Feb 13, 1973.

Reprint requests to 6 Broadmoor Dr, Little Rock, AR 72204 (Dr. Massey).

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ABSTRACT