Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated withArnold‐Chiaritype 1.5 malformation, a case report

Author:

Tabesh Homayoun1ORCID,Riazi Ali1ORCID,Mahmoodkhani Mehdi1ORCID,Sharafi Mohammad1ORCID,Sourani Arman1ORCID,Mahdkhah Ata2ORCID,Foroughi Mina3ORCID

Affiliation:

1. Department of Neurosurgery School of Medicine, Isfahan University of Medical Sciences Isfahan Iran

2. Department of Neurosurgery Urmia University of Medical Sciences Urmia Iran

3. Isfahan Medical Students' Research Committee (IMSRC) Isfahan University of Medical Sciences Isfahan Iran

Abstract

AbstractA 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.

Publisher

Wiley

Subject

General Medicine

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