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(Referência obtida automaticamente do SciELO, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Communicative and psycholinguistic abilities in children with phenylketonuria and congenital hypothyroidism

Texto completo
Autor(es):
Mariana Germano Gejão [1] ; Amanda Tragueta Ferreira [2] ; Greyce Kelly Silva [3] ; Fernanda da Luz Anastácio-Pessan [4] ; Dionísia Aparecida Cusin Lamônica [5]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] University of São Paulo. Bauru School of Dentistry. Department of Speech-Language Pathology and Audiology - Brasil
[2] University of São Paulo. Bauru School of Dentistry. Department of Speech-Language Pathology and Audiology - Brasil
[3] Municipal Public Service. Speech Language Pathologist - Brasil
[4] the Association of Parents and Friends of Special Needs Individuals. Neonatal Screening Laboratory - Brasil
[5] University of São Paulo. Bauru School of Dentistry. Department of Speech-Language Pathology and Audiology - Brasil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: Journal of Applied Oral Science; v. 17, p. 69-75, 2009-00-00.
Resumo

The Neonatal Screening for Inborn Errors of Metabolism of the Association of Parents and Friends of Special Needs Individuals (APAE) - Bauru, Brazil, was implanted and accredited by the Brazilian Ministry of Health in 1998. It covers about 286 cities of the Bauru region and 420 collection spots. Their activities include screening, diagnosis, treatment and assistance to congenital hypothyroidism (CH) and phenylketonuria (PKU), among others. In 2005, a partnership was established with the Department of Speech-Language Pathology and Audiology, Bauru School of Dentistry, University of São Paulo, Bauru, seeking to characterize and to follow, by means of research studies, the development of the communicative abilities of children with CH and PKU. OBJECTIVE: The aim of this study was to describe communicative and psycholinguistic abilities in children with CH and PKU. MATERIALS AND METHODS: Sixty-eight children (25 children aged 1 to 120 months with PKU and 43 children aged 1 to 60 months with CH) participated in the study. The handbooks were analyzed and different instruments were applied (Observation of Communication Behavior, Early Language Milestone Scale, Peabody Picture Vocabulary Test, Gesell & Amatruda's Behavioral Development Scale, Portage Operation Inventory, Language Development Evaluation Scale, Denver Developmental Screening Test, ABFW Child Language Test-phonology and Illinois Test of Psycholinguistic Abilities), according to the children's age group and developmental level. RESULTS: It was observed that the children with PKU and CH at risk for alterations in their developmental abilities (motor, cognitive, linguistic, adaptive and personal-social), mainly in the first years of life. Alterations in the psycholinguistic abilities were also found, mainly after the preschool age. Attention deficits, language and cognitive alterations were more often observed in children with CH, while attention deficits with hyperactivity and alterations in the personal-social, language and motor adaptive abilities were more frequent in children with PKU. CONCLUSION: CH and PKU can cause communicative and psycholinguistic alterations that compromise the communication and affect the social integration and learning of these individuals, proving the need of having these abilities assisted by a speech and language pathologist. (AU)

Processo FAPESP: 07/00130-0 - Habilidades comunicativas em crianças com hipotireoidismo congênito tratadas desde o período neonatal
Beneficiário:Dionísia Aparecida Cusin Lamônica
Modalidade de apoio: Auxílio à Pesquisa - Regular