Inan, C., Sayin, N.C., Gurkan, H., Atli, E., Gursoy Erzincan, S., Uzun, I., et al. (2019) Schizencephaly Accompanied by Occipital Encephalocele and Deletion of Chromosome 22q13.32: A Case Report. Fetal and Pediatric Pathology, 38, 496-502.
https://doi.org/10.1080/15513815.2019.1604921

has been cited by the following article:

• TITLE: Schizencephaly: A Case Report and Review of Literature

  AUTHORS: Olusola P. Okunola, Olufemi K. Olaniyi, Eguaveon J. Oronsaye

  KEYWORDS: Open Lip Schizencephaly, Status Epilepticus, Seizure

  JOURNAL NAME: Open Journal of Pediatrics, Vol.12 No.5, November 3, 2022

  ABSTRACT: Schizencephaly is a rare congenital malformation of the brain that could present with repeated seizures. We report a case of a 17-year-old boy who presented with status epilepticus. Further radiological evaluation revealed unilateral open lip schizencephaly. Seizure was well controlled with anti-epileptic drug and there was no need for surgical intervention. This case highlights the need for prompt radiological evaluation of patients with seizures, especially in resource-limited settings where the high cost and non-availability of such facilities might be a major impediment.