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Pathogens. 2024 Feb 15;13(2):177. doi: 10.3390/pathogens13020177.
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Mortality from Congenital Zika Syndrome - Nationwide Cohort Study in Brazil.先天性寨卡综合征导致的死亡率——巴西全国队列研究。
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Congenital Zika Infection and the Risk of Neurodevelopmental, Neurological, and Urinary Track Disorders in Early Childhood. A Systematic Review.先天性寨卡病毒感染与儿童早期神经发育、神经和尿路疾病风险的系统评价。
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本文引用的文献

1
Long-term alterations in brain and behavior after postnatal Zika virus infection in infant macaques.婴儿恒河猴感染寨卡病毒后大脑和行为的长期改变。
Nat Commun. 2020 May 21;11(1):2534. doi: 10.1038/s41467-020-16320-7.
2
Developmental Outcomes Among Young Children With Congenital Zika Syndrome in Brazil.巴西先天性寨卡综合征幼儿的发育结果。
JAMA Netw Open. 2020 May 1;3(5):e204096. doi: 10.1001/jamanetworkopen.2020.4096.
3
Early epilepsy in children with Zika-related microcephaly in a cohort in Recife, Brazil: Characteristics, electroencephalographic findings, and treatment response.巴西累西腓队列中寨卡相关小头畸形儿童的早期癫痫:特征、脑电图表现和治疗反应。
Epilepsia. 2020 Mar;61(3):509-518. doi: 10.1111/epi.16444. Epub 2020 Feb 17.
4
Congenital Zika Syndrome in a Brazil-Paraguay-Bolivia border region: Clinical features of cases diagnosed between 2015 and 2018.巴西-巴拉圭-玻利维亚边境地区先天性寨卡综合征:2015 年至 2018 年间诊断病例的临床特征。
PLoS One. 2019 Oct 4;14(10):e0223408. doi: 10.1371/journal.pone.0223408. eCollection 2019.
5
Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice.寨卡病毒在成人脑组织中复制,并损害小鼠的突触和记忆。
Nat Commun. 2019 Sep 5;10(1):3890. doi: 10.1038/s41467-019-11866-7.
6
Delayed childhood neurodevelopment and neurosensory alterations in the second year of life in a prospective cohort of ZIKV-exposed children.在 ZIKV 暴露儿童的前瞻性队列研究中,第二年出现儿童神经发育迟缓及神经感觉改变。
Nat Med. 2019 Aug;25(8):1213-1217. doi: 10.1038/s41591-019-0496-1. Epub 2019 Jul 8.
7
Late Neurological Consequences of Zika Virus Infection: Risk Factors and Pharmaceutical Approaches.寨卡病毒感染的晚期神经后果:风险因素与药物治疗方法
Pharmaceuticals (Basel). 2019 Apr 17;12(2):60. doi: 10.3390/ph12020060.
8
Motor function in children with congenital Zika syndrome.先天性寨卡综合征患儿的运动功能。
Dev Med Child Neurol. 2020 Feb;62(2):221-226. doi: 10.1111/dmcn.14227. Epub 2019 Apr 4.
9
Epileptic spasms as the presenting seizure type in a patient with a new "O" of TORCH, congenital Zika virus infection.癫痫性痉挛作为先天性寨卡病毒感染这一新型TORCH感染源患者的首发癫痫发作类型。
Epilepsy Behav Case Rep. 2018 Oct 18;11:1-3. doi: 10.1016/j.ebcr.2018.09.002. eCollection 2019.
10
Epilepsy Profile in Infants with Congenital Zika Virus Infection.先天性寨卡病毒感染婴儿的癫痫概况
N Engl J Med. 2018 Aug 30;379(9):891-892. doi: 10.1056/NEJMc1716070.

神经发育、癫痫及先天性寨卡综合征患儿的药物治疗方法:一项为期两年的随访研究结果。

Neurological Development, Epilepsy, and the Pharmacotherapy Approach in Children with Congenital Zika Syndrome: Results from a Two-Year Follow-up Study.

机构信息

Centro Especializado em Reabilitação, Associação de Pais e Amigos dos Excepcionais, Campo Grande 79050-140, Brazil.

Programa de Pós-Graduação em Doenças Infecciosas e Parasitárias, Universidade Federal de Mato Grosso do Sul, Campo Grande 79070-900, Brazil.

出版信息

Viruses. 2020 Sep 25;12(10):1083. doi: 10.3390/v12101083.

DOI:10.3390/v12101083
PMID:32992985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7601787/
Abstract

Clinical outcomes related to congenital Zika syndrome (CZS) include microcephaly accompanied by specific brain injuries. Among several CZS outcomes that have been described, epilepsy and motor impairments are present in most cases. Pharmacological treatment for seizures resulting from epilepsy is performed with anticonvulsant drugs, which in the long term are related to impairments in the child's neuropsychomotor development. Here, we describe the results from a two-year follow-up of a cohort of children diagnosed with CZS related to the growth of the head circumference and some neurological and motor outcomes, including the pharmacological approach, and its results in the treatment of epileptic seizures. This paper is part of a prospective cohort study carried out in the state of Mato Grosso Sul, Brazil, based on a Zika virus (ZIKV)-exposed child population. Our data were focused on the assessment of head circumference growth and some neurological and motor findings, including the description of seizure conditions and pharmacological management in two periods. Among the 11 children evaluated, 8 had severe microcephaly associated with motor impairment and/or epilepsy. Seven children were diagnosed with epilepsy. Of these, 3 had West syndrome. In four children with other forms of epilepsy, there was no pharmacological control.

摘要

与先天性寨卡综合征(CZS)相关的临床结果包括伴有特定脑损伤的小头畸形。在已描述的几种 CZS 结果中,癫痫和运动障碍在大多数情况下存在。针对癫痫引起的癫痫发作的药物治疗是使用抗惊厥药物进行的,长期以来,这些药物与儿童的神经心理运动发育受损有关。在这里,我们描述了对与头围增长相关的 CZS 诊断的儿童队列进行为期两年的随访结果,以及一些神经和运动结果,包括药物治疗方法及其在治疗癫痫发作中的结果。本文是巴西南马托格罗索州一项前瞻性队列研究的一部分,该研究基于接触寨卡病毒(ZIKV)的儿童人群。我们的数据集中在头围生长和一些神经和运动发现的评估上,包括在两个时期描述癫痫发作情况和药物管理。在评估的 11 名儿童中,8 名患有严重的小头畸形,伴有运动障碍和/或癫痫。7 名儿童被诊断患有癫痫。其中 3 名患有 West 综合征。在其他形式的癫痫中,有 4 名儿童药物治疗无法控制。