4.2 Article

Cranial Suture Biology: From Pathways to Patient Care

Journal

JOURNAL OF CRANIOFACIAL SURGERY
Volume 23, Issue 1, Pages 13-19

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/SCS.0b013e318240c6c0

Keywords

Craniosynostosis; suture mesenchymal cells; cranial suture development; fibroblast growth factor; dura mater; cranial vault

Categories

Funding

  1. National Institutes of Health, National Institute of Dental and Craniofacial Research [1 R21 DE019274-01, 1 RC2 DE020771-01]
  2. Oak Foundation
  3. Hagey Laboratory for Pediatric Regenerative Medicine
  4. National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases [1F32AR057302-01]
  5. National Endowment of Plastic Surgery

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Craniosynostosis describes the premature pathologic partial or complete fusion of 1 or more of the cranial sutures. Over the past few decades, research on craniosynostosis has progressed from gross description of deformities to an understanding of some of the molecular etiologies behind premature suture fusion. Studies on patients with syndromic craniosynostosis have resulted in the identification of several genes, molecular events, and deformational forces involved in abnormal growth and development of the cranial vault. Conservation of craniofacial development and sequence homology between humans and other species have also led to insightful discoveries in cranial suture development. In this review, we discuss the development of the cranial vault and explain the basic science behind craniosynostosis in humans as well as in animal models and how these studies may lead to future advances in craniosynostosis treatments.

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