Related Experiment Video
Updated: May 4, 2026

Intracerebroventricular and Intravascular Injection of Viral Particles and Fluorescent Microbeads into the Neonatal Brain
Published on: July 24, 2016
Congenital cytomegalovirus infection and brain clefting
Autumn L White1, Gary L Hedlund2, James F Bale1
1Division of Pediatric Neurology, Departments of Pediatrics and Neurology, The University of Utah School of Medicine, Salt Lake City, Utah.
Insights
Congenital cytomegalovirus infection in infants can cause brain abnormalities like polymicrogyria and calcifications. This study highlights cerebral cortical clefting, including schizencephaly, as a significant feature of these infections.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Human cytomegalovirus (CMV) is a leading cause of permanent neurodevelopmental disabilities in children.
- Congenital CMV infections frequently result in intracranial abnormalities such as calcifications and polymicrogyria.
- This study focuses on cerebral cortical clefting, including schizencephaly, in infants with congenital CMV.
Purpose of the Study:
- To describe the neuroimaging features of cerebral cortical clefting in children with congenital cytomegalovirus infection.
- To identify the prevalence of specific brain abnormalities associated with congenital CMV.
Main Methods:
- Retrospective review of medical records of infants and children diagnosed with congenital CMV infection.
- Analysis of neuroimaging data (CT and MRI) obtained between 1999 and 2008.
- Evaluation of 25 children with confirmed or suspected congenital CMV infection.
Main Results:
- Among 15 children with confirmed congenital CMV, 66% had polymicrogyria or abnormal gyral patterns, 33% had cleft cortical dysplasia, and 13% had schizencephaly.
- In 10 children with suspected congenital CMV, 80% had polymicrogyria, and 10% had bilateral schizencephaly with calcifications.
- Intracranial calcifications were present in 68% of the 25 infants studied.
Conclusions:
- Clefting, manifesting as cleft cortical dysplasia or schizencephaly, is a notable feature of congenital CMV infection.
- These findings underscore the importance of recognizing cortical clefting in the neuroimaging of infants with congenital CMV.
Background:
Human cytomegalovirus, a major cause of permanent neurodevelopmental disability in children, frequently produces intracranial abnormalities, including calcifications and polymicrogyria, in infants with congenital cytomegalovirus infections. This report describes the features of cerebral cortical clefting, including schizencephaly, in children with congenital cytomegalovirus infection.
Methods:
This is a retrospective review of the medical records of infants and children with congenital cytomegalovirus infection evaluated at Primary Children's Medical Center, Salt Lake City, Utah, between 1999 and 2008.
Findings:
Twenty-five children with congenital cytomegalovirus infection were identified during this 10-year period; 23 (92%) had computed tomography and 17 (68%) had magnetic resonance imaging. Imaging was obtained at a median age of 6 months (mode 1 month or less). Of 15 children with confirmed congenital infections, 10 (66%) had polymicrogyria or abnormal gyral patterns, five (33%) had cleft cortical dysplasia, and two (13%) had schizencephaly. Of 10 children with suspected congenital cytomegalovirus infection, eight (80%) had polymicrogyria, two (20%) had cleft cortical dysplasia, and one (10%) had bilateral schizencephaly with calcifications. Seventeen of the 25 infants (68%) had intracranial calcifications.
Interpretation:
These results indicate that clefting, either as cleft cortical dysplasia or schizencephaly, is an important feature of congenital cytomegalovirus infection.
Related Concept Videos
Cytomegalovirus Disease
Encephalitis l: Introduction
Brain Abscess l: Introduction
Encephalitis ll: Pathophysiology
Neurulation
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...

