dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorSpinelli, M.
dc.creatorRocha, ACD
dc.creatorGiacheti, C. M.
dc.creatorRichiericosta, A.
dc.date2014-05-20T15:23:43Z
dc.date2016-10-25T17:57:43Z
dc.date2014-05-20T15:23:43Z
dc.date2016-10-25T17:57:43Z
dc.date1995-02-27
dc.date.accessioned2017-04-05T23:43:30Z
dc.date.available2017-04-05T23:43:30Z
dc.identifierAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 60, n. 1, p. 39-43, 1995.
dc.identifier0148-7299
dc.identifierhttp://hdl.handle.net/11449/34447
dc.identifierhttp://acervodigital.unesp.br/handle/11449/34447
dc.identifier10.1002/ajmg.1320600108
dc.identifierWOS:A1995QJ65400007
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320600108
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/878371
dc.descriptionSpeech/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.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFRAGILE X SYNDROME
dc.subjectFRA-X
dc.subjectVERBAL DYSPRAXIA
dc.subjectWORD-FINDING DIFFICULTIES
dc.subjectLANGUAGE DISORDERS
dc.subjectSPECIFIC LANGUAGE DISORDERS
dc.titleWORD-FINDING DIFFICULTIES, VERBAL PARAPHASIAS, AND VERBAL DYSPRAXIA IN 10 INDIVIDUALS WITH FRAGILE-X-SYNDROME
dc.typeOtro


Este ítem pertenece a la siguiente institución