Search results for "Deafne"

showing 10 items of 75 documents

Tone perception in Mandarin-speaking school age children with otitis media with effusion.

2017

Objectives The present study explored tone perception ability in school age Mandarin-speaking children with otitis media with effusion (OME) in noisy listening environments. The study investigated the interaction effects of noise, tone type, age, and hearing status on monaural tone perception, and assessed the application of a hierarchical clustering algorithm for profiling hearing impairment in children with OME. Methods Forty-one children with normal hearing and normal middle ear status and 84 children with OME with or without hearing loss participated in this study. The children with OME were further divided into two subgroups based on their severity and pattern of hearing loss using a h…

MaleSocial Scienceslcsh:MedicineOtologyAudiologyMonauralDeafnessMandarin Chinese0302 clinical medicineHearingSociologyMedicine and Health SciencesMedicinePsychology030223 otorhinolaryngologyChildlcsh:ScienceHearing Disordersmedia_commonLanguageMultidisciplinarySchoolsmedicine.diagnostic_testPhysicsQuietQUIETPhysical ScienceslanguageSpeech PerceptionAudiometry Pure-ToneSensory PerceptionFemalemedicine.symptomAnatomyAlgorithmsResearch Articlemedicine.medical_specialtyChinaSpeech perceptionHearing lossmedia_common.quotation_subjectEducation03 medical and health sciencesPerceptionotorhinolaryngologic diseasesSpeechHumansActive listeningbusiness.industryOtitis Media with Effusionlcsh:RMiddle EarBiology and Life SciencesLinguisticsAcousticslanguage.human_languageOtorhinolaryngologyEarsCase-Control Studieslcsh:QAudiometrybusinessHead030217 neurology & neurosurgeryNeurosciencePLoS ONE
researchProduct

Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib.

1998

A Spanish family with three Usher I syndrome-affected members was linked to markers located on chromosome 11q. A search for mutations on the myosin VIIA gene revealed a novel mutation (Cys628STOP) on exon 16 segregating with the disorder in a homozygous state. This nonsense mutation could be responsible for the disease since it leads to a truncated protein that presumably has no function.

MaleUsher syndromeNonsense mutationDNA Mutational AnalysisGenes RecessiveBiologyDeafnessMyosinsPolymerase Chain ReactionExonotorhinolaryngologic diseasesmedicineHumansCysteineMolecular BiologyGenePolymorphism Single-Stranded ConformationalGeneticsMyosin VIIaChromosomeDyneinsCell BiologyDNAExonsSyndromeMiddle Agedmedicine.diseasePedigreeMyosin VIIaMutation (genetic algorithm)MutationCodon TerminatorFemaleNovel mutationRetinitis PigmentosaMolecular and cellular probes
researchProduct

Sudden sensorineural hearing loss associated with inner ear lesions detected by magnetic resonance imaging.

2017

Although recent advances in magnetic resonance imaging (MRI) techniques have contributed to the detection of tiny lesions in the internal auditory canal (IAC) that may be responsible for sudden sensorineural hearing loss (SSNHL), there have been relatively few studies on the clinical characteristics of intra-labyrinthine hemorrhage (ILH) and labyrinthitis versus those regarding IAC tumors. Our purpose was to investigate the frequency of those IAC lesions on MRI and their clinical characteristics. Initial MRIs of 200 patients with SSNHL (93 men, 107 women; mean age = 48.61 years, range: 18-84 years), as well as detailed clinical histories, audiological examinations, and thyroid function, lip…

Malelcsh:MedicineOtologyAudiologyDeafnessPathology and Laboratory MedicineVascular MedicineDiagnostic Radiology0302 clinical medicineVertigoMedicine and Health Sciences030223 otorhinolaryngologylcsh:ScienceHearing DisordersParesisAged 80 and overMultidisciplinarymedicine.diagnostic_testbiologyRadiology and ImagingAudiologyMiddle AgedPrognosisMagnetic Resonance ImagingInner EarVertigoFemaleRadiologymedicine.symptomThyroid functionAnatomyResearch ArticleAdultmedicine.medical_specialtyBenign paroxysmal positional vertigoAdolescentHearing lossImaging TechniquesHearing Loss SensorineuralHemorrhageResearch and Analysis Methods03 medical and health sciencesLabyrinthitisYoung AdultSigns and SymptomsDiagnostic Medicinemedicineotorhinolaryngologic diseasesHumansAgedbusiness.industrylcsh:RBiology and Life SciencesMagnetic resonance imagingbiology.organism_classificationmedicine.diseaseOtorhinolaryngologyEarsEar InnerLesionslcsh:QAudiometrybusinessHead030217 neurology & neurosurgeryPloS one
researchProduct

Cerebral lateralisation during signed and spoken language production in children born deaf

2019

Highlights • Children born deaf show typical left-hemisphere dominance during language production. • No evidence of an association between left-lateralisation and language proficiency. • Exposure to auditory speech via a cochlear implant is not a prerequisite for left hemisphere language dominance.

Malelcsh:QP351-495Deafnessmusculoskeletal systemArticlelcsh:Neurophysiology and neuropsychologyotorhinolaryngologic diseasesCochlear implantsHumansfTCDFemaleSign languageChildDominance Cerebralhuman activitiesDeafChildrenLateralisationLanguageFunctional transcranial Doppler sonographyDevelopmental Cognitive Neuroscience
researchProduct

Waking and dreaming: Related but structurally independent. Dream reports of congenitally paraplegic and deaf-mute persons

2011

Models of dream analysis either assume a continuum of waking and dreaming or the existence of two dissociated realities. Both approaches rely on different methodology. Whereas continuity models are based on content analysis, discontinuity models use a structural approach. In our study, we applied both methods to test specific hypotheses about continuity or discontinuity. We contrasted dream reports of congenitally deaf-mute and congenitally paraplegic individuals with those of non-handicapped controls. Continuity theory would predict that either the deficit itself or compensatory experiences would surface in the dream narrative. We found that dream form and content of sensorially limited pe…

Malemedia_common.quotation_subjectExperimental and Cognitive PsychologyDeafnessContinuity theoryDevelopmental psychologyYoung AdultArts and Humanities (miscellaneous)Surveys and QuestionnairesPerceptionDevelopmental and Educational PsychologyHumansNarrativeWakefulnessDreamContent (Freudian dream analysis)media_commonParaplegiaModalitieshumanitiesDreamsContent analysisFemaleConsciousnessPsychologypsychological phenomena and processesCognitive psychologyConsciousness and Cognition
researchProduct

The Jervell and Lange-Nielsen syndrome.

1991

Deafness and electrocardiographic changes (prolongation of the Q-T interval and inversion of the T wave) with a clinical picture of syncopal attacks and sudden death, were described as a distinct syndrome by Jervell and Lange-Nielsen in 1957. The syndrome is inherited as an autosomal recessive trait. In this study, all the cases reported since 1957 and their proposed prevalence are reviewed. The authors describe the 4 cases they have studied, all of which presented congenital sensorineural hearing loss and electrocardiographic changes characteristic of the syndrome. The relatively high number of cases they have encountered casts doubt on literature that states that the syndrome occurs more …

Malemedicine.medical_specialtyPediatricsHeart diseaseElectrodiagnosisDeafnessSudden deathAutosomal recessive traitElectrocardiographyAudiometryLange-nielsen syndromemedicineCongenital sensorineural hearing lossHumansmedicine.diagnostic_testbusiness.industryInfantGeneral Medicinemedicine.diseaseSurgeryJervell and Lange-Nielsen syndromeLong QT SyndromeOtorhinolaryngologyPediatrics Perinatology and Child HealthFemalebusinessElectrocardiographyInternational journal of pediatric otorhinolaryngology
researchProduct

Working Memory Function in Children with Single Side Deafness Using a Bone-Anchored Hearing Implant: A Case-Control Study

2018

The importance of a good hearing function to preserve memory and cognitive abilities has been shown in the adult population, but studies on the pediatric population are currently lacking. This study aims at evaluating the effects of a bone-anchored hearing implant (BAHI) on speech perception, speech processing, and memory abilities in children with single side deafness (SSD). We enrolled <i>n</i> = 25 children with SSD and assessed them prior to BAHI implantation, and at 1-month and 3-month follow-ups after BAHI implantation using tests of perception in silence and perception in phonemic confusion, dictation in silence and noise, and working memory and short-term memory function…

Malemedicine.medical_specialtySpeech perceptionAdolescentPhysiologymedia_common.quotation_subjectAudiologyDeafnessBone anchored hearing aidsHearing Loss Unilateral03 medical and health sciencesSpeech and Hearing0302 clinical medicineHearing AidsNormal hearingMemoryPerceptionotorhinolaryngologic diseasesmedicineHumans030223 otorhinolaryngologyChildmedia_commonSingle side deafneDictationBone-Anchored ProsthesisWorking memoryHearing TestsOtorhinolaryngology2734 Pathology and Forensic MedicineSpeech perceptionCognitionBone-anchored hearing implant; Memory; Normal hearing; Single side deafness; Speech perception;Speech processingSensory SystemsSilenceMemory Short-TermOtorhinolaryngologyBone-anchored hearing implantSingle Side DeafnessCase-Control StudiesChild PreschoolFemaleImplant3616Sensory SystemPsychologyNoise030217 neurology & neurosurgery
researchProduct

E-ABR in Patients with Cochlear Implant: A Comparison between Patients with Malformed Cochlea and Normal Cochlea

2019

Objectives This study aims to compare the electrical auditory brainstem response (EABR) following cochlear implant (CI) surgery in pediatric subjects with cochlear malformation and a normal cochlea, in order to assess the sensitivity of EABR and to evaluate the surgery outcome. Materials and methods A total of 26 pediatric subjects who were deaf and scheduled for CI surgery were enrolled into this case control study. Group A (n=20) included subjects with a normo-conformed cochlea. Group B (n=6) included subjects with cochlear malformation. Subjects were evaluated with EABR immediately (T0) and 6 months (T1) post-CI surgery. The EABR Waves III and V average amplitude and latency were compare…

Malemedicine.medical_specialtymedicine.medical_treatmentOtoacoustic Emissions SpontaneousEABRCochlear nerve conductionDeafnessAudiologyABRPostoperative ComplicationsCochlear malformationCochlear implantEvoked Potentials Auditory Brain StemReaction Timeotorhinolaryngologic diseasesHumansMedicineIn patientCochlear implantCochlear NerveCochleamedicine.diagnostic_testbusiness.industrySignificant differenceInfantMagnetic resonance imagingGeneral MedicineCochlear malformationlcsh:OtorhinolaryngologyMagnetic Resonance Imaginglcsh:RF1-547CochleaSettore MED/32 - AudiologiaCochlear ImplantsSettore MED/31 - OtorinolaringoiatriaAuditory brainstem responseOtorhinolaryngologyCase-Control StudiesChild PreschoolSurgery outcomeFemaleOriginal ArticleABR; Cochlear implant; Cochlear malformation; Cochlear nerve conduction; EABR;Tomography X-Ray Computedbusiness
researchProduct

Boosting syntax training with temporally regular musical primes in children with cochlear implants

2018

International audience; Objectives : Previous research has suggested the use of rhythmic structures (implemented in musical material) to improve linguistic structure processing (i.e., syntax processing), in particular for populations showing deficits in syntax and temporal processing (e.g., children with developmental language disorders). The present study proposes a long-term training program to improve syntax processing in children with cochlear implants, a population showing syntax processing deficits in perception and production.Methods : The training program consisted of morphosyntactic training exercises (based on speech processing) that were primed by musical regular primes (8 sessio…

Malemedicine.medical_treatmentRhythmDeafness0302 clinical medicineCochlear implantRepetition PrimingTask Performance and AnalysisOrthopedics and Sports MedicineAttentionCochlear implantChildeducation.field_of_studyCross-Over Studies4. Education05 social sciencesRehabilitationhumanitiesChild Preschool[ SCCO.NEUR ] Cognitive science/NeuroscienceGrammaticalityFemalePsychologyCognitive psychologyPopulationRepetition priming050105 experimental psychology03 medical and health sciencesTemporal attentionMemory[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologymedicineHumansSpeech0501 psychology and cognitive sciencesSyntaxeducationMusic TherapyCommunicationbusiness.industryMusical syntax[SCCO.NEUR]Cognitive science/NeuroscienceLinguisticsSpeech processingSyntaxComprehensionCochlear ImplantsAcoustic Stimulationbusiness030217 neurology & neurosurgery[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologyMusic
researchProduct

Keypoints to Successful Newborn Hearing Screening. Thirty Years of Experience and Innovations

2021

Congenital deafness is a major pediatric problem, affecting about 1.5–3 per 1000 newborns. The early treatment through cochlear implantation and auditory rehabilitation has been a historic milestone. Early diagnosis of congenital deafness is an essential requirement to obtain the best results, which is achieved through neonatal screening, a diagnostic practice that we began systematically at the Hospital Clínico in Valencia (Spain) 30 years ago. Neonatal hearing screening is successful in most developed countries. Its implementation has been slow due to the multiple difficulties that its universal application entails since it involves several health professionals and must be carried out, in…

Newborn screeningHealth professionalsnewborn screeningLeadership and Managementbusiness.industryHealth PolicyRAuditory rehabilitationHealth InformaticsReviewotoacoustic emissionsmedicine.diseaseneonatal hearing screeningHearing screeningHealth Information ManagementdeafnessMilestone (project management)MedicineMedicineMedical emergencybusinessCochlear implantationDeveloped countryHealthcare
researchProduct