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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorSILVA, Liliane Aparecida Fagundes
dc.contributor.authorKIM, Chong Ae
dc.contributor.authorMATAS, Carla Gentile
dc.date.accessioned2018-10-11T19:05:21Z
dc.date.available2018-10-11T19:05:21Z
dc.date.issued2018
dc.identifier.citationCODAS, v.30, n.5, p.e20170267, 2018
dc.identifier.issn2317-1782
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/28739
dc.description.abstractABSTRACT Purpose Identify the characteristics of the clinical audiological evaluation of individuals with Williams syndrome by means of a systematic literature review. Research strategies The following research question was initially determined: “What are the characteristics of clinical auditory assessment in individuals with Williams syndrome?”. From this, a bibliographic search was conducted in four databases using the descriptors: Williams syndrome, Hearing loss, and Audiology. Selection criteria Only full articles with evidence levels 1 or 2, published in Brazilian Portuguese or English, were selected. Data analysis Results obtained in the auditory tests used in the clinical routine, namely: immittance test, pure-tone audiometry, otoacoustic emissions, and brainstem auditory evoked potential were analyzed. Results Two hundred nine studies were found, but only 12 met the inclusion criteria for the study. It was possible to observe prevalence of type A tympanometry curve, which may occur with absence of acoustic reflexes, mild to moderate sensorineural hearing loss, affecting mainly the high frequencies, absent or less amplified otoacoustic emissions, and brainstem auditory evoked potential without retrocochlear alteration. Conclusion Cochlear impairment is common in individuals with Williams syndrome and the main disorders found in the hearing assessment in this population are absence of otoacoustic emissions and acoustic reflexes, as well as presence of mild to moderate sensorineural hearing loss, mainly in the high-frequency range, observed by audiometry.
dc.description.abstractRESUMO Objetivo Identificar por meio de uma revisão sistemática da literatura quais são as características da avaliação audiológica clínica de indivíduos com síndrome de Williams. Estratégia de pesquisa Inicialmente foi determinada a seguinte pergunta de pesquisa: “Quais são as características da avaliação auditiva clínica em indivíduos com síndrome de Williams?”. A partir desta, foi realizado um levantamento bibliográfico em 4 bases de dados, utilizando-se dos seguintes descritores: síndrome de Williams (Williams syndrome), perda auditiva (hearing loss) e audiologia (audiology). Critérios de seleção Foram selecionados artigos com nível de evidência 1 ou 2, publicados na íntegra nos idiomas português brasileiro ou inglês. Análise dos dados Foram analisados os resultados obtidos nos testes auditivos utilizados na rotina clínica, incluindo: imitanciometria, audiometria tonal, emissões otoacústicas e potencial evocado auditivo de tronco encefálico. Resultados 209 estudos foram encontrados, porém apenas 12 contemplaram os critérios de inclusão para o estudo. Foi possível observar prevalência de curva timpanométrica do tipo A, que pode ocorrer juntamente com ausência de reflexos acústicos, perda auditiva neurossensorial de grau leve a moderado acometendo principalmente as frequências altas, emissões otoacústicas ausentes ou de menor amplitude e potencial evocado auditivo de tronco encefálico sem alteração retrococlear. Conclusão O comprometimento coclear é comum em indivíduos com síndrome de Williams e as principais alterações na avaliação auditiva nesta população são a ausência das emissões otoacústicas e dos reflexos acústicos bem como a presença de perda auditiva neurossensorial de grau leve a moderado principalmente nas frequências altas na audiometria tonal.
dc.language.isopor
dc.language.isoeng
dc.publisherSociedade Brasileira de Fonoaudiologia
dc.relation.ispartofCoDAS
dc.rightsopenAccess
dc.subjectWilliams Syndrome
dc.subjectHearing Loss
dc.subjectCochlea
dc.subjectAudiology
dc.subjectHearing
dc.subjectSíndrome de Williams
dc.subjectPerda Auditiva
dc.subjectCóclea
dc.subjectAudiologia
dc.subjectAudição
dc.titleCaracterísticas da avaliação auditiva na síndrome de Williams: revisão sistemática
dc.title.alternativeCharacteristics of auditory evaluation in Williams syndrome: a systematic review
dc.typearticle
dc.rights.holderCopyright Sociedade Brasileira de Fonoaudiologia
dc.identifier.doi10.1590/2317-1782/20182017267
dc.identifier.pmid30231111
dc.subject.wosAudiology & Speech-Language Pathology
dc.subject.wosRehabilitation
dc.type.categoryreview
dc.type.versionpublishedVersion
hcfmusp.description.beginpagee20170267
hcfmusp.description.issue5
hcfmusp.description.volume30
hcfmusp.origemWOS
hcfmusp.origem.idSCIELO:S2317-17822018000500601
hcfmusp.origem.id2-s2.0-85055815118
hcfmusp.origem.idWOS:000449981600015
hcfmusp.relation.referenceAttias J., 2013, ENT and Audiology News, V21-6, P76
hcfmusp.relation.referenceAttias Joseph, 2008, Journal of Basic and Clinical Physiology and Pharmacology, V19, P193
hcfmusp.relation.referenceBarozzi S, 2013, EUR J MED GENET, V56, P490, DOI 10.1016/j.ejmg.2013.07.001
hcfmusp.relation.referenceBarozzi S, 2012, AM J MED GENET A, V158A, P759, DOI 10.1002/ajmg.a.35241
hcfmusp.relation.referenceBedeschi MF, 2011, AM J MED GENET A, V155A, P353, DOI 10.1002/ajmg.a.33819
hcfmusp.relation.referenceBellugi U, 2000, J COGNITIVE NEUROSCI, V12, P7, DOI 10.1162/089892900561959
hcfmusp.relation.referenceBellugi U, 2001, CLIN NEUROSCI RES, V1, P217, DOI 10.1016/S1566-2772(01)00008-1
hcfmusp.relation.referenceBEUST G, 2000, KLIN PADIATR, V212, P299
hcfmusp.relation.referenceCanales CP, 2015, EUR J HUM GENET, V23, P774, DOI 10.1038/ejhg.2014.188
hcfmusp.relation.referenceCherniske EM, 2004, AM J MED GENET A, V131A, P255, DOI 10.1002/ajmg.a.30400
hcfmusp.relation.referenceDeutsch SI, 2007, CNS SPECTRUMS, V12, P903, DOI 10.1017/S1092852900015686
hcfmusp.relation.referenceDi Rosa C., 2015, OPEN J GENETICS, V5, P12
hcfmusp.relation.referenceGagliardi C, 2007, PEDIATR NEUROL, V36, P301, DOI 10.1016/j.pediatrneurol.2007.01.001
hcfmusp.relation.referenceGothelf D, 2006, NEUROLOGY, V66, P390, DOI 10.1212/01.wnl.0000196643.35395.5f
hcfmusp.relation.referenceHolinger DP, 2005, BRAIN RES, V1037, P35, DOI 10.1016/j.brainres.2004.11.038
hcfmusp.relation.referenceHoogenraad SC, 2004, BIOESSAYS, V26, P141, DOI 10.1002/bies.10402
hcfmusp.relation.referenceJarvinen-Pasley A, 2008, DEV PSYCHOPATHOL, V20, P1, DOI 10.1017/S0954579408000011
hcfmusp.relation.referenceJarvinen-Pasley A, 2010, NEUROPSYCHOLOGIA, V48, P456, DOI 10.1016/j.neuropsychologia.2009.10.003
hcfmusp.relation.referenceJohnson LB, 2001, J OTOLARYNGOL, V30, P90, DOI 10.2310/7070.2001.20811
hcfmusp.relation.referenceKorenberg JR, 2000, J COGNITIVE NEUROSCI, V12, P89, DOI 10.1162/089892900562002
hcfmusp.relation.referenceLenhoff HM, 1997, SCI AM, V277, P68, DOI 10.1038/scientificamerican1297-68
hcfmusp.relation.referenceLenhoff HM, 2001, MUSIC PERCEPT, V18, P491, DOI 10.1525/mp.2001.18.4.491
hcfmusp.relation.referenceLense M, 2013, J INTELL DISABIL RES, V57, P850, DOI 10.1111/j.1365-2788.2012.01611.x
hcfmusp.relation.referenceLevitin DJ, 2005, J CHILD PSYCHOL PSYC, V46, P514, DOI 10.1111/j.1469-7610.2004.00376.x
hcfmusp.relation.referenceLevitin DJ, 2004, CHILD NEUROPSYCHOL, V10, P223, DOI 10.1080/09297040490909288
hcfmusp.relation.referenceLi HH, 2009, EMBO MOL MED, V1, P50, DOI 10.1002/emmm.200900003
hcfmusp.relation.referenceLucena J, 2010, BMC MED GENET, V11, DOI 10.1186/1471-2350-11-61
hcfmusp.relation.referenceMarler JA, 2005, AM J MED GENET A, V138A, P318, DOI 10.1002/ajmg.a.30970
hcfmusp.relation.referenceMarler JA, 2010, AM J MED GENET C, V154C, P249, DOI 10.1002/ajmg.c.30262
hcfmusp.relation.referenceMartens MA, 2010, NEUROPSYCHOLOGIA, V48, P2602, DOI 10.1016/j.neuropsychologia.2010.05.007
hcfmusp.relation.referenceMatsumoto Nozomu, 2011, Commun Integr Biol, V4, P208, DOI 10.4161/cib.4.2.14491
hcfmusp.relation.referenceMeng YH, 2002, NEURON, V35, P121, DOI 10.1016/S0896-6273(02)00758-4
hcfmusp.relation.referenceMeng YH, 2003, REV NEUROSCIENCE, V14, P233
hcfmusp.relation.referenceMeyer-Lindenberg A, 2006, NAT REV NEUROSCI, V7, P380, DOI 10.1038/nrn1906
hcfmusp.relation.referenceSugayama Sofia Mizuho Miura, 2007, Clinics, V62, P159, DOI 10.1590/S1807-59322007000200011
hcfmusp.relation.referencePaglialonga A, 2014, INT J PEDIATR OTORHI, V78, P1861, DOI 10.1016/j.ijporl.2014.08.010
hcfmusp.relation.referencePaglialonga A, 2011, HEARING RES, V272, P157, DOI 10.1016/j.heares.2010.10.004
hcfmusp.relation.referenceRossi Natalia Freitas, 2006, Pró-Fono R. Atual. Cient., V18, P331, DOI 10.1590/S0104-56872006000300013
hcfmusp.relation.referenceSafieddine S, 1999, EUR J NEUROSCI, V11, P803, DOI 10.1046/j.1460-9568.1999.00487.x
hcfmusp.relation.referenceScott RW, 2007, J MOL MED-JMM, V85, P555, DOI 10.1007/s00109-007-0165-6
hcfmusp.relation.referenceShah SM, 2009, NEUROSCIENCE, V164, P478, DOI 10.1016/j.neuroscience.2009.08.049
hcfmusp.relation.referenceVolterra V, 2003, DEV NEUROPSYCHOL, V23, P33, DOI 10.1207/S15326942DN231&2_3
hcfmusp.relation.referenceWengenroth M, 2010, PLOS ONE, V5, DOI 10.1371/journal.pone.0012326
hcfmusp.relation.referenceZarchi O, 2011, J PEDIATR-US, V158, P301, DOI 10.1016/j.jpeds.2010.07.056
hcfmusp.relation.referenceZarchi Omer, 2010, Isr J Psychiatry Relat Sci, V47, P125
hcfmusp.relation.reference2009, Oxford Centre for Evidence-based Medicine Levels of Evidence
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Artigos e Materiais de Revistas Científicas - FM/MFT
Departamento de Fisioterapia, Fonoaudiologia e Terapia Ocupacional - FM/MFT

Artigos e Materiais de Revistas Científicas - FM/MPE
Departamento de Pediatria - FM/MPE

Artigos e Materiais de Revistas Científicas - LIM/34
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Artigos e Materiais de Revistas Científicas - LIM/36
LIM/36 - Laboratório de Pediatria Clínica


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