scholarly journals Reply to ‘A critical analysis of neurodevelopmental and neurosensory outcomes after 2 years for children with in utero Zika virus exposure’

2019 ◽  
Vol 25 (11) ◽  
pp. 1642-1643
Author(s):  
Karin Nielsen-Saines ◽  
Patricia Brasil ◽  
Tara Kerin ◽  
Zilton Vasconcelos ◽  
Claudia Raja Gabaglia ◽  
...  
2019 ◽  
Vol 25 (11) ◽  
pp. 1641-1642 ◽  
Author(s):  
Manon Vouga ◽  
Léo Pomar ◽  
Alice Panchaud ◽  
Didier Musso ◽  
David Baud

2019 ◽  
Vol 21 (1) ◽  
pp. 12-12 ◽  
Author(s):  
Beuy Joob ◽  
Viroj Wiwanitkit
Keyword(s):  
In Utero ◽  

2019 ◽  
Vol 173 (1) ◽  
pp. 52 ◽  
Author(s):  
Sarah B. Mulkey ◽  
Dorothy I. Bulas ◽  
Gilbert Vezina ◽  
Yamil Fourzali ◽  
Armando Morales ◽  
...  
Keyword(s):  
In Utero ◽  

2018 ◽  
Vol 21 (1) ◽  
pp. 2-11 ◽  
Author(s):  
Johnathan Pierson ◽  
Rajashekar Reddy Yeruva ◽  
Rif S. El-Mallakh

2020 ◽  
Vol 174 (3) ◽  
pp. 269 ◽  
Author(s):  
Sarah B. Mulkey ◽  
Margarita Arroyave-Wessel ◽  
Colleen Peyton ◽  
Dorothy I. Bulas ◽  
Yamil Fourzali ◽  
...  

Viruses ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 325
Author(s):  
Julia A. Gomes ◽  
Eduarda Sgarioni ◽  
Juliano A. Boquett ◽  
Ana Cláudia P. Terças-Trettel ◽  
Juliana H. da Silva ◽  
...  

Zika virus (ZIKV) causes Congenital Zika Syndrome (CZS) in individuals exposed prenatally. Here, we investigated polymorphisms in VEGFA, PTGS2, NOS3, TNF, and NOS2 genes as risk factors to CZS. Forty children with CZS and forty-eight children who were in utero exposed to ZIKV infection, but born without congenital anomalies, were evaluated. Children with CZS were predominantly infected by ZIKV in the first trimester (p < 0.001) and had mothers with lower educational level (p < 0.001) and family income (p < 0.001). We found higher risk of CZS due the allele rs2297518[A] of NOS2 (OR = 2.28, CI 95% 1.17–4.50, p = 0.015). T allele and TT/CT genotypes of the TNF rs1799724 and haplotypes associated with higher expression of TNF were more prevalent in children with CZS and severe microcephaly (p = 0.029, p = 0.041 and p = 0.030, respectively). Our findings showed higher risk of CZS due ZIKV infection in the first trimester and suggested that polymorphisms in NOS2 and TNF genes affect the risk of CZS and severe microcephaly.


2021 ◽  
Vol 25 (5) ◽  
pp. 2730-2733
Author(s):  
Chongzhi Bai ◽  
Jianqing Hao ◽  
Shihua Li ◽  
George Fu Gao ◽  
Yu Nie ◽  
...  

2021 ◽  
pp. 1357633X2110631
Author(s):  
Sarah B Mulkey ◽  
Margarita Arroyave-Wessel ◽  
Colleen Peyton ◽  
Emily Ansusinha ◽  
Corina Gutierrez ◽  
...  

The COVID-19 pandemic occurred during planned neurodevelopmental follow-up of Colombian children with antenatal Zika-virus exposure. The objective of the study was to leverage the institution's telemedicine infrastructure to support international clinical child outcome research. In a prospective cohort study of child neurodevelopment (NCT04398901), we used synchronous telemedicine to remotely train a research team and perform live observational assessments of children in Sabanalarga, Colombia. An observational motor and conceptional standardized tool kit was mailed to Colombia; other materials were translated and emailed; team training was done virtually. Children were recruited by team on the ground. Synchronous activities were video-recorded directly to two laptops, each with a telehealth Zoom link to allow simultaneous evaluation of “table” and “standing” activities, and backup recordings were captured directly on the device in Colombia. The U.S. team attended live over Zoom from four states and five distinct locations, made observational notes, and provided real-time feedback. Fifty-seven, 3–4-year-old children with Zika-virus exposure and 70 non-exposed controls were studied during 10 daytrips. Direct laptop recording ensured complete record of child activities due to internet outages. Telemedicine can be used to successfully perform international neurodevelopmental outcome research in children during the COVID-19 pandemic. Telemedicine can benefit global health studies.


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