Hindawi Publishing Corporation BioMed Research International Volume 2016, Article ID 8243145, 10 pages http://dx.doi.org/10.1155/2016/8243145 Review Article Alice in Wonderland Syndrome: A Clinical and Pathophysiological Review Giulio Mastria,1 Valentina Mancini,1 Alessandro Viganò,1,2 and Vittorio Di Piero1,3 1 DepartmentofNeurologyandPsychiatry,SapienzaUniversityofRome,Rome,Italy 2Department of Anatomy, Histology, Forensic Medicine and Orthopaedics, Sapienza University of Rome, Rome, Italy 3University Consortium for Adaptive Disorders and Head Pain (UCADH), Pavia, Italy Correspondence should be addressed to Alessandro Vigano;`
[email protected] Received 13 June 2016; Accepted 20 November 2016 Academic Editor: Oliver von Bohlen und Halbach Copyright © 2016 Giulio Mastria et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Alice in Wonderland Syndrome (AIWS) is a perceptual disorder, principally involving visual and somesthetic integration, firstly reported by Todd, on the literary suggestion of the strange experiences described by Lewis Carroll in Alice in Wonderland books. Symptoms may comprise among others aschematia and dysmetropsia. This syndrome has many different etiologies; however EBV infection is the most common cause in children, while migraine affects more commonly adults. Many data support a strict relationship between migraine and AIWS, which could be considered in many patients as an aura or a migraine equivalent, particularly in children. Nevertheless, AIWS seems to have anatomical correlates. According to neuroimaging, temporoparietal- occipital carrefour (TPO-C) is a key region for developing many of AIWS symptoms. The final part of this review aims to find the relationship between AIWS symptoms, presenting a pathophysiological model.