CC BY-NC-ND 4.0 · Arq Neuropsiquiatr 2017; 75(08): 605
DOI: 10.1590/0004-282X20170104
OPINION

Congenital Zika syndrome: an epidemic of neurologic disability

Síndrome congênita do Zika: uma epidemia de desabilidade neurológica
Alex R. Paciorkowski
1   University of Rochester Medical Center, Neurogenetics Consultation Service, Departments of Neurology, Pediatrics, Biomedical Genetics, and Neuroscience, New York, USA.
› Institutsangaben

Dear Editors,

The paper by van der Linden et al., “Discordant clinical outcomes of congenital Zika virus infection in twin pregnancies”[1] provides additional information in a story that has placed Zika firmly in the company of other infections such as cytomegalovirus and toxoplasmosis that can cause birth defects in the central nervous system. Unlike these other congenital infections, however, Zika virus regularly causes a particularly severe brain phenotype, rarely seen even by specialists in brain malformations. While microcephaly, central nervous system calcifications, and abnormal gyral patterning can be observed as sequelae of other congenital infections, in the case of Zika these aspects have been notably pronounced and severe[2].

Some controversy continues to surround the diagnosis of congenital Zika syndrome, in part due to serologic cross-reactivity with Dengue virus[3]. In this report, both of the affected infants described had positive anti-Zika IgM present in the CSF, evidence that an intrauterine infection with Zika had occurred. The sudden appearance of severe microcephaly, subcortical calcifications, and extensive cortical malformations in epidemic proportions in northeastern Brazil in 2015-2016 does argue for a single etiologic infectious agent responsible for such an unusual neurologic phenotype in the population.

Many genetic causes of congenital microcephaly are recognized, and most are due to loss-of-function sequence variations in genes critical for cell cycle progression and cellular growth[4]. As a result, these genetic syndromes are often associated with a reduction in number of neuroprogenitor cells. Zika virus appears to behave in much the same way[5],[6], by targeting for infection those cells most vulnerable for injury, and whose numbers cannot be replaced.

The appearance of an infectious agent that recapitulates known genetic mechanisms for microcephaly has come at an enormous price, with over 2,000 children affected with congenital Zika syndrome in Brazil alone, and cases reported in other countries in Latin America[7]. Already, observed sequelae include epilepsy, visual impairment, feeding difficulties, increased susceptibility to respiratory infections, and orthopedic complications. These children require complex multidisciplinary care, and the long-term social and economic effects of this outbreak have yet to be written.



Publikationsverlauf

Eingereicht: 29. Juni 2017

Angenommen: 06. Juli 2017

Artikel online veröffentlicht:
05. September 2023

© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Linden VV, Linden Junior HV, Leal MC, Rolim Filho EL, Linden AV, Aragão MFVV et al. Discordant clinical outcomes of congenital Zika virus infection in twin pregnancies. Arq Neuropsiquiatr. 2017;75(6):381-6. https://doi.org/10.1590/0004-282X20170066
  • 2 Del Campo M, Feitosa IML, Ribeiro EM, Horovitz DDG, Pessoa ALS, França GVA et al. The phenotypic spectrum of congenital Zika syndrome. Am J Med Genet A. 2017;173(4):841-57. https://doi.org/10.1002/ajmg.a.38170
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  • 6 Brault J-B, Khou C, Basset J, Coquand L, Fraisier V, Frenkiel M-P et al. Comparative analysis between flaviviruses reveals specific neural stem cell tropism for zika virus in the mouse developing neocortex. EBioMedicine. 2016;10:71-6. https://doi.org/10.1016/j.ebiom.2016.07.018
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