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HERO ID
7436087
Reference Type
Journal Article
Title
Chiari I Malformation and Craniosynostosis
Author(s)
Turgut, M; Tubbs, RS; ,
Year
2020
Publisher
Springer International Publishing
Location
Cham
Book Title
The Chiari Malformations
Page Numbers
239-259
DOI
10.1007/978-3-030-44862-2_20
URL
http://link.springer.com/10.1007/978-3-030-44862-2_20
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Abstract
Hindbrain hernia is often seen in various craniosynostoses. Although these can be seen in single-suture craniosynostosis, syndromic craniosynostosis has a greater risk of having Chiari malformation type I (CM I). In particular, patients with Apert and Crouzon syndromes should be investigated for CM I. Today, simultaneous or consecutive cranial vault remodeling and suboccipital decompression are standard treatments in these complex patients with combined craniosynostosis and CM I, but further studies are needed because of the complexity of surgical care.
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