Childhood Neurologic Conditions: Neuroanatomic Abnormalities

Anthony Fine1, Katherine M Schupack2

  • 1Mayo Clinic Rochester Department of Neurology, 200 First St SW Floor 8, Rochester, MN 55905.

FP Essentials
|December 2, 2022
PubMed

Insights

Abnormal infant head shape and size require careful evaluation. Differentiating positional plagiocephaly from craniosynostosis is crucial for timely intervention and preventing complications like increased intracranial pressure.

Area of Science:

  • Pediatric Neurology
  • Craniofacial Surgery
  • Developmental Pediatrics

Background:

  • Abnormal head shape and size are commonly observed in infants.
  • Positional plagiocephaly is a skull deformation without suture fusion, distinct from craniosynostosis.

Purpose of the Study:

  • To highlight the importance of differentiating positional plagiocephaly from craniosynostosis.
  • To emphasize the need for early specialist referral in craniosynostosis cases.
  • To define microcephaly and macrocephaly and their potential etiologies.

Main Methods:

  • Clinical observation and physical examination are primary diagnostic tools.
  • Differential diagnosis between positional plagiocephaly and craniosynostosis is essential.
  • Evaluation of head circumference for microcephaly and macrocephaly.

Main Results:

  • Craniosynostosis requires prompt neurosurgical or craniofacial specialist intervention to prevent skull deformity and intracranial pressure.
  • Microcephaly and macrocephaly have diverse etiologies including genetic and metabolic disorders.
  • Rapid head size increase may indicate hydrocephalus, necessitating urgent assessment.

Conclusions:

  • Accurate diagnosis of infant head shape abnormalities is critical for appropriate management.
  • Early identification and intervention for conditions like craniosynostosis and hydrocephalus improve patient outcomes.
  • Understanding the range of head size variations and their causes guides clinical decision-making.

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