Posterior reversible encephalopathy syndrome in two Omani children with underlying renal diseases

Mohamed A. El-Naggari*, Dana Al-Nabhani, Ibtisam El-Nour, Alaa El-Manzalawy, Anas Alwogud A. Abdelmogheth

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)e424-e428
JournalSultan Qaboos University Medical Journal
Issue number3
Publication statusPublished - 2015


  • Case report
  • Magnetic resonance imaging
  • Oman
  • Pediatrics
  • Peritoneal dialysis
  • Posterior reversible encephalopathy syndrome
  • Systemic lupus erythematosus

ASJC Scopus subject areas

  • General Medicine


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