Early Intervention in Fragile X Syndrom

Detalhes bibliográficos
Autor(a) principal: Apolónio, Ana
Data de Publicação: 2012
Outros Autores: Franco, Vitor
Tipo de documento: Artigo de conferência
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/5281
Resumo: The Fragile X syndrome, although not very frequent, is the most common inherited cause of mental retardation and is very often associated with autism spectrum disorders. In this presentation will be presented the most frequent motor, speech and social characteristics of the development of children with this syndrome. The importance of a diagnosis is associated with the possibility of early intervention. Will be analyzed how different studies have identified the main contributions of early intervention services for the child, the family and the context. The search for specific characteristics of the work with this syndrome will be made from the presentation of a case followed by a EI team.
id RCAP_80d805296e281c2b89b61d34b81478ce
oai_identifier_str oai:dspace.uevora.pt:10174/5281
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Early Intervention in Fragile X SyndromSXFx fragile syndromThe Fragile X syndrome, although not very frequent, is the most common inherited cause of mental retardation and is very often associated with autism spectrum disorders. In this presentation will be presented the most frequent motor, speech and social characteristics of the development of children with this syndrome. The importance of a diagnosis is associated with the possibility of early intervention. Will be analyzed how different studies have identified the main contributions of early intervention services for the child, the family and the context. The search for specific characteristics of the work with this syndrome will be made from the presentation of a case followed by a EI team.2012-09-19T11:37:01Z2012-09-192012-09-13T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjecthttp://hdl.handle.net/10174/5281http://hdl.handle.net/10174/5281porsimnaonaondvfranco@uevora.pt684Apolónio, AnaFranco, Vitorinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T18:43:48Zoai:dspace.uevora.pt:10174/5281Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:00:17.052390Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Early Intervention in Fragile X Syndrom
title Early Intervention in Fragile X Syndrom
spellingShingle Early Intervention in Fragile X Syndrom
Apolónio, Ana
SXF
x fragile syndrom
title_short Early Intervention in Fragile X Syndrom
title_full Early Intervention in Fragile X Syndrom
title_fullStr Early Intervention in Fragile X Syndrom
title_full_unstemmed Early Intervention in Fragile X Syndrom
title_sort Early Intervention in Fragile X Syndrom
author Apolónio, Ana
author_facet Apolónio, Ana
Franco, Vitor
author_role author
author2 Franco, Vitor
author2_role author
dc.contributor.author.fl_str_mv Apolónio, Ana
Franco, Vitor
dc.subject.por.fl_str_mv SXF
x fragile syndrom
topic SXF
x fragile syndrom
description The Fragile X syndrome, although not very frequent, is the most common inherited cause of mental retardation and is very often associated with autism spectrum disorders. In this presentation will be presented the most frequent motor, speech and social characteristics of the development of children with this syndrome. The importance of a diagnosis is associated with the possibility of early intervention. Will be analyzed how different studies have identified the main contributions of early intervention services for the child, the family and the context. The search for specific characteristics of the work with this syndrome will be made from the presentation of a case followed by a EI team.
publishDate 2012
dc.date.none.fl_str_mv 2012-09-19T11:37:01Z
2012-09-19
2012-09-13T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/conferenceObject
format conferenceObject
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/5281
http://hdl.handle.net/10174/5281
url http://hdl.handle.net/10174/5281
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv sim
nao
nao
nd
vfranco@uevora.pt
684
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799136485320949760

Registros relacionados