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Alice in Wonderland syndrome: a novel neurological presentation of Zika virus infection

  • Alberto E. Paniz-Mondolfi(corresponding author)
    ,
  • José Giraldo
    ,
  • ,
  • Oriana Pacheco
    ,
  • Germán Y. Lombó-Lucero
    ,
  • Juan D. Plaza
*Corresponding author for this work
  • Instituto de Estudios Avanzados (IDEA)
    ,
  • Instituto de Investigaciones Biomédicas IDB/Incubadora Venezolana de la Ciencia
    ,
  • Instituto de Biomedicina / Instituto Venezolano de los Seguros Sociales (IVSS)
    ,
  • Hospital Internacional Barquisimeto
    ,
  • Universidad Tecnológica de Pereira
    ,
  • Colombian Collaborative Network on Zika and other Arboviruses (RECOLZIKA)
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 660-663 (4 pages)

Journal (Volume, Issue Number)

Journal of NeuroVirology (Volume 24, Issue 5)

Publication milestones

  • Published - 01/10/2018

Publication status

Published - 01/10/2018

ISSN

1355-0284

Publication IDs

  • Scopus: 85051423375
  • PubMed: 30105501

Abstract

Zika virus (ZIKV) is a flavivirus endemic in Africa and Southern Asian countries, which has recently emerged in unprecedented epidemic proportions around the world. Although ZIKV infection is often asymptomatic or distinguished by non-specific influenza-like symptoms, an increase in its pathogenicity and biological behavior has been the hallmark of the current pandemic. Increasing evidence suggests that neurotropic strains of ZIKV have evolved from less pathogenic strains of the virus. Neurological manifestations of ZIKV infection include a spectrum of congenital and non-congenital clinical entities, however visual somatosensory perceptual disorders have not been recorded to date. Herein, we report a case of a 15-year-old female who presented with a constellation of perceptual symptoms (metamorphopsia, telopsia, and pelopsia) following acute ZIKV infection. Although such symptoms may have originated from direct viral injury, a post-ZIKV autoimmune reaction to previously unexposed neuronal surface antigens or through molecular mimicry cannot be excluded. The development of Alice in Wonderland syndrome in our patient highlights the ever-increasing expanding spectrum of neurological symptoms associated to ZIKV infection.

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