CRANIOSYNOSTOSIS – PATHOGENESIS, CLASSIFICATION AND CLINICAL CONSEQUENCES

Authors

  • Khakimov M.N. Author

Keywords:

Keywords: craniosynostosis, premature suture fusion, skull deformity, FGFR mutations, pediatric neurosurgery, intracranial pressure, syndromic craniosynostosis

Abstract

Abstract: Craniosynostosis is a congenital disorder characterized by the premature fusion of one or more cranial sutures, resulting in abnormal skull growth and potential impairment of brain development. The condition may occur as an isolated anomaly or as part of a genetic syndrome. Early diagnosis and optimal management are crucial to prevent increased intracranial pressure, neurodevelopmental delay, and aesthetic deformities. This article reviews the epidemiology, pathogenesis, classification, clinical manifestations, and potential complications of craniosynostosis.

References

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4. Kimonis V, Gold JA, Hoffman TL, Panchal J. Genetics of craniosynostosis. American Journal of Medical Genetics Part A. 2007;143A:305–320.

5. Morriss-Kay GM, Wilkie AOM. Growth of the normal skull vault and its alteration in craniosynostosis. Birth Defects Research Part C. 2005;75(4):253–267.

Published

2025-12-10

How to Cite

Khakimov M.N. (2025). CRANIOSYNOSTOSIS – PATHOGENESIS, CLASSIFICATION AND CLINICAL CONSEQUENCES. JOURNAL OF NEW CENTURY INNOVATIONS, 90(2), 84-85. https://journalss.org/index.php/new/article/view/9270