Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/239804 |
Resumo: | Five years after the identification of Zika virus as a human teratogen, we reviewed the early clinical manifestations, collectively called congenital Zika syndrome (CZS). Children with CZS have a very poor prognosis with extremely low performance in motor, cognitive, and language development domains, and practically all feature severe forms of cerebral palsy. However, these manifestations are the tip of the iceberg, with some children presenting milder forms of deficits. Additionally, neurodevelopment can be in the normal range in the majority of the non-microcephalic children born without brain or eye abnormalities. Vertical transmission and the resulting disruption in development of the brain are much less frequent when maternal infection occurs in the second half of the pregnancy. Experimental studies have alerted to the possibility of other behavioral outcomes both in prenatally infected children and in postnatal and adult infections. Cofactors play a vital role in the development of CZS and involve genetic, environmental, nutritional, and social determinants leading to the asymmetric distribution of cases. Some of these social variables also limit access to multidisciplinary professional treatment. |
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Faccini, Lavinia SchulerBoquett, Juliano AndréKowalski, Thayne WoycinckGerzson, Laís RodriguesAlmeida, Carla Skilhan deSanti, LucéliaSilva, Walter Orlando Beys daQuincozes-Santos, AndréGomes, Julia do AmaralVianna, Fernanda Sales LuizFraga, Lucas RosaRosa, Rafael Lopes daAbeche, Alberto MantovaniSouza, Diogo Onofre Gomes de2022-06-07T04:39:12Z20221664-8021http://hdl.handle.net/10183/239804001141096Five years after the identification of Zika virus as a human teratogen, we reviewed the early clinical manifestations, collectively called congenital Zika syndrome (CZS). Children with CZS have a very poor prognosis with extremely low performance in motor, cognitive, and language development domains, and practically all feature severe forms of cerebral palsy. However, these manifestations are the tip of the iceberg, with some children presenting milder forms of deficits. Additionally, neurodevelopment can be in the normal range in the majority of the non-microcephalic children born without brain or eye abnormalities. Vertical transmission and the resulting disruption in development of the brain are much less frequent when maternal infection occurs in the second half of the pregnancy. Experimental studies have alerted to the possibility of other behavioral outcomes both in prenatally infected children and in postnatal and adult infections. Cofactors play a vital role in the development of CZS and involve genetic, environmental, nutritional, and social determinants leading to the asymmetric distribution of cases. Some of these social variables also limit access to multidisciplinary professional treatment.application/pdfengFrontiers in genetics. Lausanne. Vol. 13 (Mar. 2022), 758715, 18 p.Infecção por Zika virusManifestações neurológicasTranstornos do neurodesenvolvimentoCriançaDeficiências do desenvolvimentoMicrocephalyZika (ZIKV)EpilepsyCerebral palsyNeurodevelopementEyeNeurodevelopment in children exposed to Zika in utero : clinical and molecular aspectsEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001141096.pdf.txt001141096.pdf.txtExtracted Texttext/plain110707http://www.lume.ufrgs.br/bitstream/10183/239804/2/001141096.pdf.txt0549f6d3ebc9876e8b194834c8f0f1beMD52ORIGINAL001141096.pdfTexto completo (inglês)application/pdf2822426http://www.lume.ufrgs.br/bitstream/10183/239804/1/001141096.pdf918dec76e9578488ccee311260b44805MD5110183/2398042024-01-11 04:24:56.556204oai:www.lume.ufrgs.br:10183/239804Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-01-11T06:24:56Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
title |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
spellingShingle |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects Faccini, Lavinia Schuler Infecção por Zika virus Manifestações neurológicas Transtornos do neurodesenvolvimento Criança Deficiências do desenvolvimento Microcephaly Zika (ZIKV) Epilepsy Cerebral palsy Neurodevelopement Eye |
title_short |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
title_full |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
title_fullStr |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
title_full_unstemmed |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
title_sort |
Neurodevelopment in children exposed to Zika in utero : clinical and molecular aspects |
author |
Faccini, Lavinia Schuler |
author_facet |
Faccini, Lavinia Schuler Boquett, Juliano André Kowalski, Thayne Woycinck Gerzson, Laís Rodrigues Almeida, Carla Skilhan de Santi, Lucélia Silva, Walter Orlando Beys da Quincozes-Santos, André Gomes, Julia do Amaral Vianna, Fernanda Sales Luiz Fraga, Lucas Rosa Rosa, Rafael Lopes da Abeche, Alberto Mantovani Souza, Diogo Onofre Gomes de |
author_role |
author |
author2 |
Boquett, Juliano André Kowalski, Thayne Woycinck Gerzson, Laís Rodrigues Almeida, Carla Skilhan de Santi, Lucélia Silva, Walter Orlando Beys da Quincozes-Santos, André Gomes, Julia do Amaral Vianna, Fernanda Sales Luiz Fraga, Lucas Rosa Rosa, Rafael Lopes da Abeche, Alberto Mantovani Souza, Diogo Onofre Gomes de |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Faccini, Lavinia Schuler Boquett, Juliano André Kowalski, Thayne Woycinck Gerzson, Laís Rodrigues Almeida, Carla Skilhan de Santi, Lucélia Silva, Walter Orlando Beys da Quincozes-Santos, André Gomes, Julia do Amaral Vianna, Fernanda Sales Luiz Fraga, Lucas Rosa Rosa, Rafael Lopes da Abeche, Alberto Mantovani Souza, Diogo Onofre Gomes de |
dc.subject.por.fl_str_mv |
Infecção por Zika virus Manifestações neurológicas Transtornos do neurodesenvolvimento Criança Deficiências do desenvolvimento |
topic |
Infecção por Zika virus Manifestações neurológicas Transtornos do neurodesenvolvimento Criança Deficiências do desenvolvimento Microcephaly Zika (ZIKV) Epilepsy Cerebral palsy Neurodevelopement Eye |
dc.subject.eng.fl_str_mv |
Microcephaly Zika (ZIKV) Epilepsy Cerebral palsy Neurodevelopement Eye |
description |
Five years after the identification of Zika virus as a human teratogen, we reviewed the early clinical manifestations, collectively called congenital Zika syndrome (CZS). Children with CZS have a very poor prognosis with extremely low performance in motor, cognitive, and language development domains, and practically all feature severe forms of cerebral palsy. However, these manifestations are the tip of the iceberg, with some children presenting milder forms of deficits. Additionally, neurodevelopment can be in the normal range in the majority of the non-microcephalic children born without brain or eye abnormalities. Vertical transmission and the resulting disruption in development of the brain are much less frequent when maternal infection occurs in the second half of the pregnancy. Experimental studies have alerted to the possibility of other behavioral outcomes both in prenatally infected children and in postnatal and adult infections. Cofactors play a vital role in the development of CZS and involve genetic, environmental, nutritional, and social determinants leading to the asymmetric distribution of cases. Some of these social variables also limit access to multidisciplinary professional treatment. |
publishDate |
2022 |
dc.date.accessioned.fl_str_mv |
2022-06-07T04:39:12Z |
dc.date.issued.fl_str_mv |
2022 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/239804 |
dc.identifier.issn.pt_BR.fl_str_mv |
1664-8021 |
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001141096 |
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http://hdl.handle.net/10183/239804 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Frontiers in genetics. Lausanne. Vol. 13 (Mar. 2022), 758715, 18 p. |
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info:eu-repo/semantics/openAccess |
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openAccess |
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