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dc.contributor.authorPaniagua, Lauren Medeirospt_BR
dc.contributor.authorDorfman, Maria Elza Kazumi Yamagutipt_BR
dc.contributor.authorLavinsky, Luizpt_BR
dc.contributor.authorSleifer, Pricilapt_BR
dc.date.accessioned2015-03-12T01:57:48Zpt_BR
dc.date.issued2013pt_BR
dc.identifier.issn1809-4864pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/111923pt_BR
dc.description.abstractBackground Harboyan syndrome, defined as congenital corneal dystrophy associated with progressive sensorineural hearing loss, was first described by Harboyan in 1971. It is a hereditary disease manifested by eye lesions consistent with corneal endothelial dystrophy and progressive sensorineural hearing loss. There is bilateral symmetric progressive hearing loss, which may be either dominant or recessive. Objective To report a case of a patient with a diagnosis of Harboyan syndrome. Case Report A 25-year-old woman with profound bilateral sensorineural hearing loss, showing poor hearing performance while using a personal sound amplification device, underwent hearing rehabilitation with a cochlear implant. Conclusion Rehabilitation was imperative in this case. The cochlear implant has proven to be the best therapeutic option, providing the patient with a better quality of life.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofInternational archives of otorhinolaryngology. São Paulo. Vol. 17, no. 4 (2013), p. 403-406.pt_BR
dc.rightsOpen Accessen
dc.subjectEnvelhecimentopt_BR
dc.subjectCochlear implantsen
dc.subjectHearing lossen
dc.subjectDistúrbios da audiçãopt_BR
dc.subjectSensorineuralen
dc.subjectRehabilitation of speech and language disordersen
dc.titleRehabilitation with cochlear implant in patient with Harboyan Syndromept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000930112pt_BR
dc.type.originNacionalpt_BR


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