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Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold-Chiari type 1.5 malformation, a case report. | LitMetric

A 6-year-old girl with persistent headaches and the visual problem was diagnosed as a delayed onset cranial pansynostosis with concurrent type 1.5 Arnold-Chiari malformation. She underwent multi-sutural reconstructive surgery and followed. The headache was greatly decreased and tonsillar-brain stem herniation and syrinx were resolved.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986723PMC
http://dx.doi.org/10.1002/ccr3.6981DOI Listing

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