Longitudinal assessment of visual development in non-syndromic craniosynostosis: a 1-year pre- and post-surgical

G Vasco1, G Baranello, D Ricci

  • 1Pediatric Neurology Unit, Catholic University, Rome, Italy.

Insights

Surgical correction of single-suture non-syndromic craniosynostosis significantly improves visual function in infants. Most children experienced enhanced visual acuity and oculomotor behavior post-surgery, indicating delayed visual maturation.

Area of Science:

  • Pediatric Ophthalmology
  • Craniofacial Surgery
  • Developmental Neuroscience

Background:

  • Single-suture non-syndromic craniosynostosis involves premature fusion of cranial sutures, potentially impacting neurodevelopment.
  • Visual function abnormalities can occur in affected infants, necessitating thorough pre- and post-operative assessment.

Purpose of the Study:

  • To longitudinally investigate visual function in infants with single-suture non-syndromic craniosynostosis before and after surgical correction.
  • To identify specific visual deficits and their resolution patterns following surgical intervention.

Main Methods:

  • A cohort of 29 infants (12 sagittal, 10 trigonocephaly, 7 anterior plagiocephaly) underwent comprehensive visual function testing.
  • Assessments included ocular behavior, acuity, visual fields, and fixation shift, conducted pre-surgery and at 2, 6, and 12 months post-surgery.

Main Results:

  • Pre-surgery, only 16% of infants exhibited normal visual function across all parameters.
  • Twelve months post-surgery, 65% of infants demonstrated normal visual function.
  • Post-operative abnormalities were primarily related to oculomotor behavior in infants with plagiocephaly.

Conclusions:

  • Surgical correction of single-suture non-syndromic craniosynostosis is associated with significant improvements in infant visual function.
  • The observed visual improvements suggest delayed visual maturation rather than persistent abnormalities in most cases.
  • Oculomotor function requires continued attention, particularly in infants with plagiocephaly.
Abstract