Chiari Type I malformation yielded to the diagnosis of Crouzon syndrome
Year: 2014
Type: article
Study design: Case Report
Abstract: Chiari malformation Type I (CM-I) related to syndromic craniosynostosis in pediatric patients has been well-studied. The surgical management consists of cranial vault remodeling with or without posterior fossa decompression. There were also cases, in whom CM-I was diagnosed prior to the craniosynostosis in early childhood. We present a 16-year-old boy who admitted with symptoms related to CM-I. With careful examination and further genetic investigations, a diagnosis of Crouzon syndrome was made, of which the patient and his family was unaware before. The patient underwent surgery for posterior fossa decompression and followed-up for Crouzon's syndrome. To our knowledge, this is the only case report indicating a late adolescent diagnosis of Crouzon syndrome through clinical symptoms of an associated CM-I.
Authors: Aydin Canpolat, Mehmet Osman Akçakaya, Emre Altunrende, Harun Mehmet Özlü, Hakan Duman, Tuğrul Ton, Osman Akdemir
Institution: Taksim Eğitim ve Araştırma Hastanesi
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $125
OpenAlex ID: W2017696061
