Paper Contents
Abstract
Acute non-inflammatory encephalopathy with fatty liver failure is the definition of Reye syndrome, a rare and potentially fatal juvenile condition. This syndrome was first outlined by Australian pathologist R.D.K. Reye in 1963. Early in the 1970s, it became the focus of national surveillance in the United States, which resulted in strong recommendations against giving children aspirin. It often starts with vomiting and bewilderment before quickly progressing to a coma and death. This exercise discusses the etiology, pathophysiology, and clinical manifestations of Reye syndrome and emphasizes the value of an interdisciplinary approach to treatment.
Copyright
Copyright © 2024 Malarmathi. M. This is an open access article distributed under the Creative Commons Attribution License.
