Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review

Detalhes bibliográficos
Autor(a) principal: Mouzinho, Marvina Barbosa da Silva
Data de Publicação: 2021
Outros Autores: Aguiar, Rebeca Lima de Souza, Silva, Karla Camila Karla Camila Correia da
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/20122
Resumo: Spinal Muscular Amyotrophy (SMA) is a genetic disorder of autosomal recessive, degenerative neuromuscular inheritance. It mainly affects the motor neurons of the anterior horn of the spinal cord. According to the age of onset of clinical manifestations and motor impairment, EBF is classified into four types (I to IV). This literary review study aims to expose the etiology, pathophysiology, diagnosis, treatment and the importance of physical therapy intervention in patients with Spinal Muscular Amyotrophy, specifically in type I SMA. In this research, articles that were considered for inclusion criterious involved the theme with regard to physical therapy intervention in Spinal Muscular Amyotrophy type 1. The publication of the data collected took place between 2007 and 2021, in Portuguese, English and Spanish. The bibliographical survey was carried out in the following databases: Scielo, Pubmed, PEDro, Lilacs and Academic Google, from March to October. During the research, physiotherapeutic intervention was observed in Spinal Muscular Amyotrophy, specifically in type 1 SMA. Concluding that the mode of action of physiotherapy advocates minimizing/slowing down the clinical manifestations that affect the musculoskeletal system and complications in the respiratory system, contributing to promote quality and prolong life, and consequently preventing the death of these patients.
id UNIFEI_b995dca0a91b6a0735917f20c8db4b19
oai_identifier_str oai:ojs.pkp.sfu.ca:article/20122
network_acronym_str UNIFEI
network_name_str Research, Society and Development
repository_id_str
spelling Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature reviewIntervención fisioterapêutica em amiotrofia muscular espinal tipo 1: revisión de la literaturaIntervenção fisioterapêutica na amiotrofia muscular espinhal tipo 1: revisão de literaturaAME (Amiotrofia Muscular Espinhal)AME tipo IFisioterapiaReabilitação.AME (Spinal Muscular Amyotrophy)AME type IPhysiotherapyRehabilitation.AME (Amiotrofia muscular espinal)AME tipo IFisioterapiaRehabilitación.Spinal Muscular Amyotrophy (SMA) is a genetic disorder of autosomal recessive, degenerative neuromuscular inheritance. It mainly affects the motor neurons of the anterior horn of the spinal cord. According to the age of onset of clinical manifestations and motor impairment, EBF is classified into four types (I to IV). This literary review study aims to expose the etiology, pathophysiology, diagnosis, treatment and the importance of physical therapy intervention in patients with Spinal Muscular Amyotrophy, specifically in type I SMA. In this research, articles that were considered for inclusion criterious involved the theme with regard to physical therapy intervention in Spinal Muscular Amyotrophy type 1. The publication of the data collected took place between 2007 and 2021, in Portuguese, English and Spanish. The bibliographical survey was carried out in the following databases: Scielo, Pubmed, PEDro, Lilacs and Academic Google, from March to October. During the research, physiotherapeutic intervention was observed in Spinal Muscular Amyotrophy, specifically in type 1 SMA. Concluding that the mode of action of physiotherapy advocates minimizing/slowing down the clinical manifestations that affect the musculoskeletal system and complications in the respiratory system, contributing to promote quality and prolong life, and consequently preventing the death of these patients.La amiotrofia muscular espinal (AME) es un trastorno genético de herencia neuromuscular degenerativa autosómica recesiva. Afecta principalmente a las motoneuronas del asta anterior de la médula espinal. Según la edad de aparición de las manifestaciones clínicas y el deterioro motor, la LME se clasifica en cuatro tipos (I a IV). Este estudio de revisión literaria tiene como objetivo exponer la etiología, fisiopatología, diagnóstico, tratamiento y la importancia de la intervención fisioterapéutica en pacientes con Amiotrofia Muscular Espinal, específicamente en AME tipo I. En esta investigación, los artículos que fueron considerados para criterios de inclusión involucraron el tema con Respecto a la intervención de fisioterapia en Amiotrofia Muscular Espinal tipo 1. La publicación de los datos recolectados se realizó entre 2007 y 2021, en portugués, inglés y español. El relevamiento bibliográfico se realizó en las siguientes bases de datos: Scielo, Pubmed, PEDro, Lilacs y Academic Google, de marzo a octubre. Durante la investigación se observó intervención fisioterapéutica en Amiotrofia Muscular Espinal, específicamente en AME tipo 1. Concluyendo que la forma de trabajo de la fisioterapia es minimizar / retrasar las manifestaciones clínicas que afectan el sistema musculoesquelético y las complicaciones en el sistema respiratorio, contribuyendo a promover la calidad y prolongar la vida, y consecuentemente prevenir la muerte de estos pacientes.A Amiotrofia Muscular Espinhal (AME) é uma patologia de origem genética de herança autossômica recessiva, neuromuscular degenerativa. Acomete principalmente os neurônios motores do corno anterior da medula espinhal. De acordo com a idade de inicío das manifestações clinicas, e pelo comprometimento motor, a AME é classificada em quatro tipos (I a IV). O referido estudo de revisão literária tem como objetivo expor a etiologia, fisiopatologia, diagnóstico, tratamento e a importância da intervenção fisioterapêutica em pacientes portadores da Amiotrofia Muscular Espinhal, em especifico na AME tipo I. Na presente pesquisa foram considerados para criterios de inclusão artigos que envolvesse a tematica no que se refere á intervenção fisioterapêutica na Amiotrofia Muscular Espinhal tipo 1. A publicação dos dados coletados ocorreu entre o período de 2007 a 2021, em lingua portuguesa, inglesa e espanhola. O levantamento bibibliográfico foi realizado nas bases de dados: Scielo, Pubmed, PEDro, Lilacs e Google acadêmico, no período de março a outubro. No decorrer da pesquisa foi observado á intervenção fisioterapêutica na Amiotrofia Muscular Espinhal em especifico na AME tipo 1. Concluindo que o modo de atuação da fisioterapia preconiza minimizar/retardar as manifestações clínicas que afetam o sistema musculoesquelético e as complicações no sistema respiratório, contribuindo para promover qualidade e prolongar a vida, e consequentemente evitando o óbito desses pacientes.Research, Society and Development2021-09-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2012210.33448/rsd-v10i12.20122Research, Society and Development; Vol. 10 No. 12; e88101220122Research, Society and Development; Vol. 10 Núm. 12; e88101220122Research, Society and Development; v. 10 n. 12; e881012201222525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/20122/18010Copyright (c) 2021 Marvina Barbosa da Silva Mouzinho; Rebeca Lima de Souza Aguiar; Karla Camila Karla Camila Correia da Silvahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessMouzinho, Marvina Barbosa da Silva Aguiar, Rebeca Lima de Souza Silva, Karla Camila Karla Camila Correia da 2021-11-14T20:26:51Zoai:ojs.pkp.sfu.ca:article/20122Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:39:51.706016Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
Intervención fisioterapêutica em amiotrofia muscular espinal tipo 1: revisión de la literatura
Intervenção fisioterapêutica na amiotrofia muscular espinhal tipo 1: revisão de literatura
title Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
spellingShingle Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
Mouzinho, Marvina Barbosa da Silva
AME (Amiotrofia Muscular Espinhal)
AME tipo I
Fisioterapia
Reabilitação.
AME (Spinal Muscular Amyotrophy)
AME type I
Physiotherapy
Rehabilitation.
AME (Amiotrofia muscular espinal)
AME tipo I
Fisioterapia
Rehabilitación.
title_short Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
title_full Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
title_fullStr Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
title_full_unstemmed Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
title_sort Physiotherapeutic intervention in spinal muscular amyotrophy type 1: literature review
author Mouzinho, Marvina Barbosa da Silva
author_facet Mouzinho, Marvina Barbosa da Silva
Aguiar, Rebeca Lima de Souza
Silva, Karla Camila Karla Camila Correia da
author_role author
author2 Aguiar, Rebeca Lima de Souza
Silva, Karla Camila Karla Camila Correia da
author2_role author
author
dc.contributor.author.fl_str_mv Mouzinho, Marvina Barbosa da Silva
Aguiar, Rebeca Lima de Souza
Silva, Karla Camila Karla Camila Correia da
dc.subject.por.fl_str_mv AME (Amiotrofia Muscular Espinhal)
AME tipo I
Fisioterapia
Reabilitação.
AME (Spinal Muscular Amyotrophy)
AME type I
Physiotherapy
Rehabilitation.
AME (Amiotrofia muscular espinal)
AME tipo I
Fisioterapia
Rehabilitación.
topic AME (Amiotrofia Muscular Espinhal)
AME tipo I
Fisioterapia
Reabilitação.
AME (Spinal Muscular Amyotrophy)
AME type I
Physiotherapy
Rehabilitation.
AME (Amiotrofia muscular espinal)
AME tipo I
Fisioterapia
Rehabilitación.
description Spinal Muscular Amyotrophy (SMA) is a genetic disorder of autosomal recessive, degenerative neuromuscular inheritance. It mainly affects the motor neurons of the anterior horn of the spinal cord. According to the age of onset of clinical manifestations and motor impairment, EBF is classified into four types (I to IV). This literary review study aims to expose the etiology, pathophysiology, diagnosis, treatment and the importance of physical therapy intervention in patients with Spinal Muscular Amyotrophy, specifically in type I SMA. In this research, articles that were considered for inclusion criterious involved the theme with regard to physical therapy intervention in Spinal Muscular Amyotrophy type 1. The publication of the data collected took place between 2007 and 2021, in Portuguese, English and Spanish. The bibliographical survey was carried out in the following databases: Scielo, Pubmed, PEDro, Lilacs and Academic Google, from March to October. During the research, physiotherapeutic intervention was observed in Spinal Muscular Amyotrophy, specifically in type 1 SMA. Concluding that the mode of action of physiotherapy advocates minimizing/slowing down the clinical manifestations that affect the musculoskeletal system and complications in the respiratory system, contributing to promote quality and prolong life, and consequently preventing the death of these patients.
publishDate 2021
dc.date.none.fl_str_mv 2021-09-14
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/20122
10.33448/rsd-v10i12.20122
url https://rsdjournal.org/index.php/rsd/article/view/20122
identifier_str_mv 10.33448/rsd-v10i12.20122
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/20122/18010
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. 12; e88101220122
Research, Society and Development; Vol. 10 Núm. 12; e88101220122
Research, Society and Development; v. 10 n. 12; e88101220122
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
_version_ 1797052689151950848