Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/23438 |
Resumo: | Objective: To characterize the microcephaly cases in the west region of Mato Grosso presumably by the congenital Zika virus syndrome. Methods: It is a descriptive study, retrospective in longitudinal design. The study included children with microcephaly presumably by the congenital Zika virus syndrome. The selected variables were the epidemiological profile with sociodemographic data, growth monitoring by the cephalic perimeter evolution, length, weight and body mass index. Results: 12 patients were included in the research. Five children were born with congenital microcephaly and six developed the condition after birth. The cephalic perimeter evolved in an inappropriate way only in the first semester of life, with a growth rate of 0.72 cm/month and being the normal rate 1.5cm/month. The most found complications were tetraparetic cerebral paralysis (91,66%), global delay in neuropsychomotor development (91,66%), epilepsy (58,33%) and pyramidal syndrome (50%). Some findings rarely observed in the literature were found in the research like West syndrome, superior sagittal sinus dilation and single lateral ventricles. All of then presented neuroimaging exam alterations. The most found were pachygyria (66,67%), ventriculomegaly (58,34%) and subcortical calcifications (41,66%). Conclusions: The recognition of the onset phenotype in the congenital Zika virus syndrome will help to ensure an appropriate etiological evaluation and an adequate multi-professional continuous monitoring of these affected children. |
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Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso Caracterización de niños con microcefalia presumida por virus congénito del síndrome de zika de la región oeste de Mato Grosso Caracterização de crianças com microcefalia presumidamente por síndrome congênita do Zika vírus da região oeste de Mato Grosso Zika virusCongenital malformationsMicrocephaly.Virus zikaMalformaciones congénitasMicrocefalia.Zika vírusMalformações congênitasMicrocefalia.Objective: To characterize the microcephaly cases in the west region of Mato Grosso presumably by the congenital Zika virus syndrome. Methods: It is a descriptive study, retrospective in longitudinal design. The study included children with microcephaly presumably by the congenital Zika virus syndrome. The selected variables were the epidemiological profile with sociodemographic data, growth monitoring by the cephalic perimeter evolution, length, weight and body mass index. Results: 12 patients were included in the research. Five children were born with congenital microcephaly and six developed the condition after birth. The cephalic perimeter evolved in an inappropriate way only in the first semester of life, with a growth rate of 0.72 cm/month and being the normal rate 1.5cm/month. The most found complications were tetraparetic cerebral paralysis (91,66%), global delay in neuropsychomotor development (91,66%), epilepsy (58,33%) and pyramidal syndrome (50%). Some findings rarely observed in the literature were found in the research like West syndrome, superior sagittal sinus dilation and single lateral ventricles. All of then presented neuroimaging exam alterations. The most found were pachygyria (66,67%), ventriculomegaly (58,34%) and subcortical calcifications (41,66%). Conclusions: The recognition of the onset phenotype in the congenital Zika virus syndrome will help to ensure an appropriate etiological evaluation and an adequate multi-professional continuous monitoring of these affected children.Objetivo: caracterizar casos de microcefalia en el oeste de Mato Grosso, presuntamente debido al síndrome congénito del virus del Zika. Método: Estudio descriptivo, retrospectivo en un diseño longitudinal. Se incluyeron en el estudio niños con microcefalia presuntamente debida al síndrome congénito del virus del Zika. Las variables seleccionadas fueron el perfil epidemiológico con datos sociodemográficos, seguimiento del crecimiento mediante el análisis de la evolución del perímetro cefálico, longitud, peso e índice de masa corporal. Resultados: se incluyeron 12 pacientes en el estudio. Cinco niños nacieron con microcefalia congénita y seis desarrollaron microcefalia posnatal. El perímetro cefálico evolucionó de manera inadecuada solo en el primer semestre de vida, donde la tasa fue de 0,72 cm / mes y la ideal es de 1,5 cm / mes. Las complicaciones más frecuentes fueron parálisis cerebral tetraparética (91,66%), retraso global del desarrollo neuropsicomotor (91,66%), epilepsia (58,33%) y síndrome piramidal (50%). Hallazgos poco observados en la literatura y encontrados en el estudio fueron síndrome de West, dilatación del seno sagital superior y ventrículos laterales únicos. Todos mostraron alteraciones en el examen de neuroimagen. Las más frecuentes fueron paquigiria (66,67%), ventriculomegalia (58,34%) y calcificaciones subcorticales (41,66%). Conclusión: El reconocimiento del fenotipo de la participación del síndrome congénito del virus del Zika ayudará a garantizar una evaluación etiológica adecuada y un seguimiento multiprofesional continúo apropiado de estos niños afectados.Objetivo: Caracterizar os casos de microcefalia da região oeste de Mato Grosso presumidamente pela síndrome congênita do Zika vírus. Método: Estudo descritivo, retrospectivo em desenho longitudinal. Foram incluídos no estudo crianças com microcefalia presumidamente pela síndrome congênita do Zika vírus. As variáveis selecionadas foram o perfil epidemiológico com dados sociodemográficos, monitorização do crescimento por meio da análise da evolução do perímetro cefálico, do comprimento, do peso e do índice de massa corporal. Resultados: 12 pacientes foram incluídos no estudo. Cinco crianças nasceram com microcefalia congênita e seis desenvolveram microcefalia pós-natal. O perímetro cefálico evoluiu de forma inadequada apenas no primeiro semestre de vida, onde a taxa foi de 0.72 cm/mês e o ideal é 1.5 cm/mês. As complicações mais encontradas foram paralisia cerebral tetraparética (91.66%), atraso global no desenvolvimento neuropsicomotor (91.66%), epilepsia (58.33%) e síndrome piramidal (50%). Achados pouco observados na literatura e encontrados no estudo foram síndrome de West, dilatação do seio sagital superior e ventrículos laterais únicos. Todos apresentaram alterações no exame de neuroimagem. O mais encontrado foi paquigiria (66.67%), ventriculomegalia (58.34%) e calcificações subcorticais (41.66%). Conclusão: O reconhecimento do fenótipo de acometimento da síndrome congênita do Zika vírus ajudará a garantir uma avaliação etiológica apropriada e um acompanhamento multiprofissional contínuo adequado dessas crianças afetadas.Research, Society and Development2021-12-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2343810.33448/rsd-v10i16.23438Research, Society and Development; Vol. 10 No. 16; e42101623438Research, Society and Development; Vol. 10 Núm. 16; e42101623438Research, Society and Development; v. 10 n. 16; e421016234382525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/23438/20693Copyright (c) 2021 Eduardo Baltazar Niesciur Lopes; Simone Galli Rocha Bragato; Fabíola Beppu Muniz Ramsdorf; Juliana Ferreira Ura Berlangahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessLopes, Eduardo Baltazar Niesciur Bragato, Simone Galli Rocha Ramsdorf, Fabíola Beppu Muniz Berlanga, Juliana Ferreira Ura 2021-12-20T11:03:07Zoai:ojs.pkp.sfu.ca:article/23438Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:42:18.468133Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso Caracterización de niños con microcefalia presumida por virus congénito del síndrome de zika de la región oeste de Mato Grosso Caracterização de crianças com microcefalia presumidamente por síndrome congênita do Zika vírus da região oeste de Mato Grosso |
title |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
spellingShingle |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso Lopes, Eduardo Baltazar Niesciur Zika virus Congenital malformations Microcephaly. Virus zika Malformaciones congénitas Microcefalia. Zika vírus Malformações congênitas Microcefalia. |
title_short |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
title_full |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
title_fullStr |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
title_full_unstemmed |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
title_sort |
Characterization of children with microcephaly presumed by congenital virus zika syndrome from the west region of Mato Grosso |
author |
Lopes, Eduardo Baltazar Niesciur |
author_facet |
Lopes, Eduardo Baltazar Niesciur Bragato, Simone Galli Rocha Ramsdorf, Fabíola Beppu Muniz Berlanga, Juliana Ferreira Ura |
author_role |
author |
author2 |
Bragato, Simone Galli Rocha Ramsdorf, Fabíola Beppu Muniz Berlanga, Juliana Ferreira Ura |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Lopes, Eduardo Baltazar Niesciur Bragato, Simone Galli Rocha Ramsdorf, Fabíola Beppu Muniz Berlanga, Juliana Ferreira Ura |
dc.subject.por.fl_str_mv |
Zika virus Congenital malformations Microcephaly. Virus zika Malformaciones congénitas Microcefalia. Zika vírus Malformações congênitas Microcefalia. |
topic |
Zika virus Congenital malformations Microcephaly. Virus zika Malformaciones congénitas Microcefalia. Zika vírus Malformações congênitas Microcefalia. |
description |
Objective: To characterize the microcephaly cases in the west region of Mato Grosso presumably by the congenital Zika virus syndrome. Methods: It is a descriptive study, retrospective in longitudinal design. The study included children with microcephaly presumably by the congenital Zika virus syndrome. The selected variables were the epidemiological profile with sociodemographic data, growth monitoring by the cephalic perimeter evolution, length, weight and body mass index. Results: 12 patients were included in the research. Five children were born with congenital microcephaly and six developed the condition after birth. The cephalic perimeter evolved in an inappropriate way only in the first semester of life, with a growth rate of 0.72 cm/month and being the normal rate 1.5cm/month. The most found complications were tetraparetic cerebral paralysis (91,66%), global delay in neuropsychomotor development (91,66%), epilepsy (58,33%) and pyramidal syndrome (50%). Some findings rarely observed in the literature were found in the research like West syndrome, superior sagittal sinus dilation and single lateral ventricles. All of then presented neuroimaging exam alterations. The most found were pachygyria (66,67%), ventriculomegaly (58,34%) and subcortical calcifications (41,66%). Conclusions: The recognition of the onset phenotype in the congenital Zika virus syndrome will help to ensure an appropriate etiological evaluation and an adequate multi-professional continuous monitoring of these affected children. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-12-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/23438 10.33448/rsd-v10i16.23438 |
url |
https://rsdjournal.org/index.php/rsd/article/view/23438 |
identifier_str_mv |
10.33448/rsd-v10i16.23438 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/23438/20693 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 10 No. 16; e42101623438 Research, Society and Development; Vol. 10 Núm. 16; e42101623438 Research, Society and Development; v. 10 n. 16; e42101623438 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052759413882880 |