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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/34447
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dc.contributor.authorSpinelli, M.-
dc.contributor.authorRocha, ACD-
dc.contributor.authorGiacheti, C. M.-
dc.contributor.authorRichiericosta, A.-
dc.date.accessioned2014-05-20T15:23:43Z-
dc.date.accessioned2016-10-25T17:57:43Z-
dc.date.available2014-05-20T15:23:43Z-
dc.date.available2016-10-25T17:57:43Z-
dc.date.issued1995-02-27-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320600108-
dc.identifier.citationAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 60, n. 1, p. 39-43, 1995.-
dc.identifier.issn0148-7299-
dc.identifier.urihttp://hdl.handle.net/11449/34447-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/34447-
dc.description.abstractSpeech/language disorders are common in the fragile X syndrome. [Howard-Peebles, 1979: Am J Hom Genet 31:214-222; Renier et al., 1983: J Ment Defic Res 27:51-59; Sparks, 1984: Birth Defects and Speech-Language Disorders, pp, 39-43; Hanson et al., 1986: Am J Med Genet 23:195-206]. Verbal paraphasias have been considered a rare feature and word-finding difficulties have seldom been reported. Here we report on ten Brazilian patients who were evaluated for speech/language disturbances and found that word-finding difficulties were present in 50% of the cases, which is a slightly higher frequency than that of clear dyspraxia. We suggest, therefore, that word-finding difficulties and verbal dyspraxia can be a common feature within the spectrum of this syndrome. Additional speech findings are discussed. (C) 1995 Wiley-Liss, Inc.en
dc.format.extent39-43-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectFRAGILE X SYNDROMEpt
dc.subjectFRA-Xpt
dc.subjectVERBAL DYSPRAXIApt
dc.subjectWORD-FINDING DIFFICULTIESpt
dc.subjectLANGUAGE DISORDERSpt
dc.subjectSPECIFIC LANGUAGE DISORDERSpt
dc.titleWORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROMEen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionPontifícia Universidade Católica de São Paulo (PUC-SP)-
dc.description.affiliationUNIV ESTADUAL PAULISTA,FAC S CAMILO,MARILIA,SP,BRAZIL-
dc.description.affiliationUNIV SAO PAULO,HOSP PESQUISA & REABILITACAO LESOES LABIO PALATAI,BAURU,SP,BRAZIL-
dc.description.affiliationPONTIFICIA UNIV CATOLICA SAO PAULO,DIV EDUC & REABILITACAO DISTURBIOS COMUNICACAO,SAO PAULO,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,FAC S CAMILO,MARILIA,SP,BRAZIL-
dc.identifier.doi10.1002/ajmg.1320600108-
dc.identifier.wosWOS:A1995QJ65400007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Medical Genetics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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