Rotavirus is an important cause of severe gastroenteritis in infants and children. Generally, rotavirus infections are self-limiting benign diseases but occasionally can cause a wide range of neurological manifestations, including benign febrile or afebrile convulsions, meningoencephalitis, cerebellitis, and lethal encephalitis or encephalopathy [1]. However, it is unclear how rotavirus can affect the central nervous system without direct invasion. Posterior reversible encephalopathy syndrome (PRES) is a well-recognized clinical disorder with typical neuroimaging findings consisting of mostly transient bilateral gray and white matter abnormalities in the posterior cerebral hemispheric regions and cerebellum [2]. The common clinical symptoms are headache, confusion, seizures, and visual disturbances such as cortical blindness. These symptoms usually recover without sequelae following appropriate treatment. Common precipitants are sudden elevations of blood pressure, renal failure, fluid restriction, and treatment with immunosuppressive drugs such as cyclosporine [3]. Recently, studies related to infection-associated PRES have been published [2,4]. We describe the case of a 6-year-old boy with rotavirus gastroenteritis who developed clinical and radiological manifestations consistent with PRES.