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.

Pediatric Neurology
|December 31, 2013
PubMed

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.
Abstract

Related Concept Videos

Cytomegalovirus Disease01:27

Cytomegalovirus Disease

Cytomegalovirus (CMV) disease is caused by human cytomegalovirus, a double-stranded DNA virus of the Herpesviridae family. While primary CMV infection is often asymptomatic in immunocompetent individuals, the virus can cause severe disease in neonates and immunocompromised patients. CMV is the most common cause of congenital viral infection in the United States, and a major pathogen in solid organ and hematopoietic stem cell transplant recipients.CMV is transmitted via bodily fluids, sexual...
102
Encephalitis l: Introduction01:19

Encephalitis l: Introduction

Encephalitis is inflammation of the brain parenchyma, most often due to infections or autoimmune processes. It presents with neuropsychiatric features such as fever, altered mental status, behavioral changes, cognitive dysfunction, seizures, focal deficits, and sometimes autonomic instability. In some cases, the meninges are also involved, resulting in meningoencephalitis.Infectious CausesInfectious encephalitis is most commonly viral but can also result from bacterial, fungal, or parasitic...
15
Brain Abscess l: Introduction01:26

Brain Abscess l: Introduction

A brain abscess is a focal, intracerebral infection characterized by a localized collection of pus within the brain parenchyma, resulting from microbial invasion and the body’s inflammatory response. It progresses through stages: early and late cerebritis, followed by early and late capsule formation, reflecting tissue destruction, immune response, and eventual encapsulation.Etiology and PathogenesisCausative organisms vary with source and host factors, often involving polymicrobial...
21
Encephalitis ll: Pathophysiology01:26

Encephalitis ll: Pathophysiology

Encephalitis is inflammation of the brain parenchyma caused by direct viral invasion or immune-mediated mechanisms triggered by infections or tumors. Both processes lead to neuronal injury, disrupted neurotransmission, and diverse neurological symptoms, often with overlapping clinical and pathological features.Autoimmune EncephalitisIn autoimmune encephalitis, antibodies target neuronal antigens on cell surfaces, synapses, or within neurons. A key example is anti-NMDAR encephalitis, which can...
22
Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the...
40.2K
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
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,...
1.1K