Affiliations 

  • 1 Klinik Kesihatan Pengkalan Kubor, Tumpat, Kelantan, Malaysia
  • 2 Department of Family Medicine, Universiti Sains Malaysia, Kubang Kerian, Malaysia, Email: [email protected]
  • 3 Department of Family Medicine, Universiti Sains Malaysia, Kubang Kerian, Malaysia
  • 4 Department of Radiology, Universiti Sains Malaysia, Kubang Kerian, Malaysia
Malays Fam Physician, 2020;15(3):90-94.
PMID: 33329869

Abstract

Schizencephaly is a very rare congenital birth defect. It is characterized by a cortical brain malformation that manifests as a grey-matter-lined cleft extending from the ependyma to the pia mater. It is a rare condition, and few cases have been reported in the literature. The exact cause is unknown. Herein, we report a case of an infant presenting with left side hemiparesis. The CT scan of her brain revealed right fronto-temporal and left parieto-temporal open-lip schizencephaly; thus, urgent referral to a pediatric neurologist was made for early intervention.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.