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Diffusion Tensor Imaging and Fiber Tractography in Children with Craniosynostosis Syndromes

BACKGROUND AND PURPOSE: Patients with craniosynostosis syndromes caused by mutations in FGFR-2, FGFR-3, and TWIST1 genes are characterized by having prematurely fused skull sutures and skull base synchondroses, which result in a skull deformity and are accompanied by brain anomalies, including alter...

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Pubblicato in:AJNR Am J Neuroradiol
Autori principali: Rijken, B.F.M., Leemans, A., Lucas, Y., van Montfort, K., Mathijssen, I.M.J., Lequin, M.H.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society of Neuroradiology 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7964691/
https://ncbi.nlm.nih.gov/pubmed/25953762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A4301
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