Craniosynostosis is often classified as nonsyndromic or syndromic. Nonsyndromic craniosynostosis is the most common type of craniosynostosis, and its cause is unknown.
However, syndromic craniosynostosis is a complication caused by certain genetic syndromes, such as Apert syndrome, Pfeiffer syndrome and Crouzon syndrome, which can affect your baby's skull development. [1,p41;3,p3] Besides craniosynostosis, other conditions also may accompany such syndromes — including hand and foot deformities, dental abnormalities, and heart problems.
Sept. 09, 2016
- Burokas L. Craniosynostosis: Caring for infants and their families. Critical Care Nurse. 2013;33:39.
- Craniosynostosis information page. National Institute of Neurological Disorders and Stroke. http://www.ninds.nih.gov/disorders/craniosynostosis/craniosynostosis.htm. Accessed Aug. 1, 2013.
- Buchanan EP, et al. Overview of craniosynostosis. http://www.uptodate.com/home. Accessed Aug. 1, 2013.
- Craniosynostosis and craniofacial disorders. American Association of Neurological Surgeons. http://www.aans.org/Patient%20Information/Conditions%20and%20Treatments/Craniosynostosis%20and%20Craniofacial%20Disorders.aspx. Accessed Aug. 1, 2013.
- Cook AJ. Decision Support System. Mayo Clinic, Rochester, Minn. June 21, 2013.