CNS Malformations in the Newborn

Kristin Barañano1, Irina Burd2

  • 1Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. kwb@jhmi.edu.

Insights

Structural brain anomalies are common findings in fetuses and neonates. Early detection and comprehensive surveillance are crucial for identifying associated conditions and guiding appropriate medical interventions.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Medical Imaging

Background:

  • Structural brain anomalies are frequently identified during prenatal or postnatal evaluations.
  • These malformations arise from disruptions in fetal brain development due to various etiological factors.
  • Associated anomalies and specific investigations are often necessary for affected fetuses and neonates.

Purpose of the Study:

  • To outline the commonality and detection of structural brain anomalies.
  • To categorize brain malformations based on perturbed developmental processes.
  • To emphasize the importance of comprehensive surveillance and further investigations for affected infants.

Main Methods:

  • Review of current literature on prenatal and postnatal detection of brain malformations.
  • Characterization of brain anomalies based on underlying etiological factors (environmental, infectious, genetic).
  • Guidelines for surveillance and diagnostic workup in fetuses and neonates with brain malformations.

Main Results:

  • Structural brain anomalies are a significant finding in pediatric neurology.
  • Etiologies include environmental, infectious, disruptive, and genetic factors impacting brain development.
  • Associated anomalies necessitate a multidisciplinary approach to management.

Conclusions:

  • Early detection of structural brain anomalies is critical.
  • A thorough evaluation for co-existing anomalies is essential.
  • Tailored investigations, including genetic testing and specialized examinations, guide management strategies.