Nonsyndromic craniosynostosis occurs when there is an early fusion of the cranial sutures in the absence of a known genetic syndrome. Traditionally, open vault remodeling has been the treatment of choice. However, in patients younger than 4-6 months, spring-mediated cranioplasty is an option for the treatment of sagittal craniosynostosis. The procedure involves minimally invasive strip craniectomy with placement of two springs and bone autograft. The spring distractors are left in for three months and subsequently removed in a second short procedure. The case highlights the work-up and management of an infant with nonsyndromic sagittal craniosynostosis.
Authors: Benjamin Googe, MD; Nicole K. Le, MPH; Ian C. Hoppe, MD
Subspecialty: Craniofacial
Disclaimer: The content and CPT codes included in this case report are accurate up to and on the publication date. Please note that CPT codes may change; and the ones included are specific to this case at the time of publication. It is recommended that you check with the appropriate coding resources for the most current codes and application.
For medical disclaimer, privacy policy, and system requirements click here.