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Updated: Jan 13, 2026

Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
Published on: November 20, 2015
Síndrome de encefalopatía posterior reversible en un niño con glomerulonefritis asociada a leptospira: el marco de
Bing Chan Shu1, Caisha Moses2,3
1Emergency Department, Sarawak General Hospital, Kuching, Malaysia.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is an under-recognised cause of seizures in children, often obscured by concurrent infections. We report a girl in her middle childhood with recurrent seizures following a week of fever and flood exposure. Initial suspicion was leptospira encephalitis, supported by positive serology. However, progressive hypertension and CT brain findings confirmed PRES secondary to leptospira-associated acute glomerulonephritis. She improved with antihypertensives, antiepileptics and antibiotics, and was discharged seizure-free. This case highlights the risk of anchoring bias and introduces the '3 P's of PRES' framework-Pressure, Pattern and Pictures-for earlier recognition and management.
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