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Posterior Reversible Encephalopathy Syndrome in Two Omani Children with Underlying Renal Diseases
Mohamed A El-Naggari1, Dana Al-Nabhani1, Ibtisam El-Nour1
1Departments of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
Insights
Posterior reversible encephalopathy syndrome (PRES) is a neurological condition often linked to hypertension. Prompt diagnosis and management, aided by MRI, are crucial for preventing permanent neurological damage in pediatric cases.
Area of Science:
- Neurology
- Pediatrics
- Radiology
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological disorder characterized by specific clinical and radiological findings.
- PRES typically presents with symptoms such as headaches, confusion, seizures, visual disturbances, and altered consciousness.
- Classic MRI findings include subcortical and cortical edema, predominantly in the posterior brain regions.
Purpose of the Study:
- To report two pediatric cases of PRES associated with underlying renal diseases.
- To highlight the role of hypertension as a significant risk factor in pediatric PRES.
- To emphasize the importance of MRI in diagnosing and prognosticating PRES.
Main Methods:
- Case report of two pediatric patients presenting with PRES.
- Review of clinical symptoms, radiological findings (MRI), and underlying conditions.
- Documentation of treatment and follow-up outcomes.
Main Results:
- Two pediatric patients with PRES and renal diseases (systemic lupus erythematosus and nephrotic syndrome) were identified.
- Both patients were hypertensive and received blood pressure control medication.
- No residual neurological deficits were observed at follow-up.
Conclusions:
- Hypertension is a critical risk factor in pediatric PRES.
- Magnetic resonance imaging (MRI) is an essential tool for PRES diagnosis and prognosis.
- Timely diagnosis and aggressive management are vital to prevent irreversible neurological damage.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is a neurological condition with a combination of clinical and radiological features. Clinical symptoms include headaches, confusion, seizures, disturbed vision or an altered level of consciousness. Classic magnetic resonance imaging (MRI) findings indicate subcortical and cortical oedema, affecting mainly the posterior cerebral region. We report two paediatric cases of PRES with underlying renal diseases presenting at the Sultan Qaboos University Hospital in Muscat, Oman, in April 2010 and August 2011. The first case was an 11-year-old girl diagnosed with systemic lupus erythematosus and the second was a six-and-a-half-year-old boy on peritoneal dialysis due to multi-drug-resistant nephrotic syndrome. Both patients were hypertensive and treated with blood pressure control medications. No residual neurological dysfunction was noted in the patients at a one-year follow-up and at discharge, respectively. The role of hypertension in paediatric PRES cases, among other important risk factors, is emphasised. Additionally, MRI is an important diagnostic and prognostic tool. Prompt diagnosis and aggressive management is fundamental to preventing permanent neurological damage.
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