Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report

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...

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Autores principales: Tabesh, Homayoun, Riazi, Ali, Mahmoodkhani, Mehdi, Sharafi, Mohammad, Sourani, Arman, Mahdkhah, Ata, Foroughi, Mina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986723/
https://www.ncbi.nlm.nih.gov/pubmed/36891239
http://dx.doi.org/10.1002/ccr3.6981
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author Tabesh, Homayoun
Riazi, Ali
Mahmoodkhani, Mehdi
Sharafi, Mohammad
Sourani, Arman
Mahdkhah, Ata
Foroughi, Mina
author_facet Tabesh, Homayoun
Riazi, Ali
Mahmoodkhani, Mehdi
Sharafi, Mohammad
Sourani, Arman
Mahdkhah, Ata
Foroughi, Mina
author_sort Tabesh, Homayoun
collection PubMed
description 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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spelling pubmed-99867232023-03-07 Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report Tabesh, Homayoun Riazi, Ali Mahmoodkhani, Mehdi Sharafi, Mohammad Sourani, Arman Mahdkhah, Ata Foroughi, Mina Clin Case Rep Case Report 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. John Wiley and Sons Inc. 2023-03-06 /pmc/articles/PMC9986723/ /pubmed/36891239 http://dx.doi.org/10.1002/ccr3.6981 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Tabesh, Homayoun
Riazi, Ali
Mahmoodkhani, Mehdi
Sharafi, Mohammad
Sourani, Arman
Mahdkhah, Ata
Foroughi, Mina
Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title_full Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title_fullStr Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title_full_unstemmed Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title_short Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report
title_sort surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with arnold‐chiari type 1.5 malformation, a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986723/
https://www.ncbi.nlm.nih.gov/pubmed/36891239
http://dx.doi.org/10.1002/ccr3.6981
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