Search results for "Hearing lo"

showing 10 items of 220 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
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Mutations in the PDS Gene in German Families with Pendred’s Syndrome: V138F Is a Founder Mutation

2003

Pendred's syndrome, an autosomal-recessive condition characterized by congenital sensorineural hearing loss and goiter, is caused by mutations in the PDS gene. Located on chromosome 7q22-q31, it encodes a chloride-iodide transporter expressed in the thyroid, inner ear, and kidney. We investigated the PDS gene of six affected individuals from four unrelated families with Pendred's syndrome by direct sequencing. PDS mutations were identified in homozygous or compound heterozygous state in all six cases. A homozygous missense mutation leading to the amino acid substitution S133T was detected in a family of Turkish origin. The mutations found in the other affected individuals, who originate fro…

MaleThreoninemedicine.medical_specialtyAdolescentTurkeyHearing Loss SensorineuralEndocrinology Diabetes and MetabolismClinical BiochemistryMutation MissenseBiologyCompound heterozygositymedicine.disease_causeBiochemistryGenetic determinismEndocrinologyHypothyroidismGermanyInternal medicineSerinemedicineHumansMissense mutationAlleleChildPendred syndromeGeneticsMutationBase SequenceBiochemistry (medical)HaplotypeInfant NewbornMembrane Transport Proteinsfood and beveragesSyndromemedicine.diseaseFounder EffectPedigreeEndocrinologyAmino Acid SubstitutionHaplotypesSulfate TransportersChild PreschoolMicrosatelliteFemaleCarrier ProteinsThe Journal of Clinical Endocrinology & Metabolism
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Sudden sensorineural hearing loss: is there a relationship between routine haematological parameters and audiogram shapes?

2016

Objective: To investigate the relationship between haematological routine parameters and audiogram shapes in patients affected by sudden sensorineural hearing loss (SSNHL). Design: A retrospective study. All patients were divided into four groups according to the audiometric curve and mean values of haematological parameters (haemoglobin, white blood cell, neutrophils and lymphocytes relative count, platelet count, haematocrit, prothrombin time, activated partial thromboplastin time, fibrinogen and neutrophil-to-lymphocite ratio) of each group were statistically compared. The prognostic role of blood profile and coagulation test was also examined. Study sample: A cohort of 183 SSNHL patient…

MaleTime FactorsNeutrophilshaematological parameterAudiologyLanguage and LinguisticsHemoglobinsLeukocyte Count0302 clinical medicineHearingLymphocytes030223 otorhinolaryngologyHematologic Testsmedicine.diagnostic_testComplete blood countAudiogramSudden sensorineural hearing lossMiddle AgedSettore MED/32 - AudiologiaTreatment OutcomeSettore MED/31 - Otorinolaringoiatriamedicine.anatomical_structureHematocrit030220 oncology & carcinogenesisCohortAudiometry Pure-ToneFemalePartial Thromboplastin TimeSteroidsmedicine.symptomPartial thromboplastin timeAdultBlood PlateletsLinguistics and Languagemedicine.medical_specialtyHearing lossHearing Loss Sensorineural03 medical and health sciencesSpeech and HearingAudiogram shapePredictive Value of TestsWhite blood cellmedicineHumansBlood CoagulationRetrospective StudiesProthrombin timePlatelet Countbusiness.industryFibrinogenAuditory ThresholdRetrospective cohort studyRecovery of FunctionHearing Loss Suddenaudiogram shape; haematological parameters; Sudden sensorineural hearing lossProthrombin TimebusinessBiomarkersInternational Journal of Audiology
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Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study

2019

The EUGEI project was supported by the grant agreement HEALTH-F2-2010-241909 from the European Community’s Seventh Framework Programme. The authors are grateful to the patients and their families for participating in the project. They also thank all research personnel involved in the GROUP project, in particular J. van Baaren, E. Veermans, G. Driessen, T. Driesen, E. van’t Hag and J. de Nijs. Bart PF Rutten was funded by a VIDI award number 91718336 from the Netherlands Scientific Organisation.

MalecannabisLogistic regression0302 clinical medicineLasso (statistics)Adverse Childhood ExperiencesStatisticsOdds RatioChild AbusePOLYGENIC RISKpsychosisChildPsychiatrySUMMER BIRTHFramingham Risk Score3. Good healthExposomePsychiatry and Mental healthmachine learningSchizophreniaArea Under CurveFemaleMarijuana UseSeasonsEnvironment And Schizophrenia—Feature Editor: Jim van OsLife Sciences & Biomedicineenvironmentpredictive modelingAdultExposomeDISORDERSrisk scoreYoung Adult03 medical and health sciencesPSYCHOSISmedicineJournal ArticleHumansHearing LossMETAANALYSISDEFICIT SCHIZOPHRENIAENVIRONMENTModels StatisticalScience & Technologychildhood traumaReceiver operating characteristicbusiness.industrySiblingsBullyingBayes TheoremChild Abuse SexualOdds ratiohearing impairmentmedicine.disease030227 psychiatryschizophreniaLogistic ModelsROC CurveSexual abuseCase-Control StudiesbusinessCHILDHOOD ADVERSITIES030217 neurology & neurosurgerywinter birth
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Association of Self-Reported Hearing Difficulty to Objective and Perceived Participation Outside the Home in Older Community-Dwelling Adults

2015

Objective: To investigate whether hearing difficulty is associated with objective and perceived participation in social and leisure activities outside the home in older adults. Method: Self-reported hearing difficulty, frequency of participation, perceived participation and Mini-Mental State Examination (MMSE) were obtained from 848 community-dwelling men and women aged 75 to 90. Results: Among persons with MMSE ≤ 24, hearing was not associated with participation. In persons with MMSE > 24, relative to persons who reported no difficulty hearing, participants with major hearing difficulty had a higher odds ratio [OR] for infrequent participation in group activities (OR 2.1, 95% confidenc…

MalekognitioGerontologysocial participationmedicine.medical_specialtymedia_common.quotation_subjectAudiologyCognitionLeisure Activitiesotorhinolaryngologic diseasesmedicineHumansautonomyHearing LossAssociation (psychology)Agedmedia_commonAged 80 and overCommunity and Home Careagingta3141CognitionOdds ratioSocial ParticipationSocial engagementConfidence intervalCross-Sectional StudieshearingFemaleIndependent LivingSelf ReportGeriatrics and GerontologyHearing difficultyPsychologyGerontologyAutonomyJournal of Aging and Health
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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
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Self-Reported Hearing Status Is Associated with Lower Limb Physical Performance, Perceived Mobility, and Activities of Daily Living in Older Communit…

2015

BACKGROUND: Poor hearing is common in older adults and it may have negative consequences which extend beyond communication. OBJECTIVES: To explore the associations of self-reported hearing problems with physical performance and self-reported difficulties in mobility and activities of daily living (ADL) in community-dwelling older adults. DESIGN: Cross-sectional cohort study SETTING: Community PARTICIPANTS: 848 men and women aged 75-90 years MEASUREMENTS: Structured face-to-face interviews to assess perceived hearing problems in the presence of noise, mobility difficulties (moving indoors, stair-climbing, 0.5 km walk and 2 km walk) and difficulties in ADLs and instrumental ADLs. The Short Ph…

Malemedicine.medical_specialtyActivities of daily livingWalkingMotor ActivityLower limbCohort StudiesDisability Evaluation03 medical and health sciences0302 clinical medicineActivities of Daily LivingOdds Ratioactivity of daily livingHumansMedicine030212 general & internal medicineCognitive skillMobility LimitationRisk factorHearing Lossta315Geriatric AssessmentPostural BalanceFinlandAgedAged 80 and overbusiness.industryagingta3141Odds ratiophysical performancemobilityCross-Sectional StudiesliikkuvuusPhysical performancehearingPhysical therapyFemaleSelf ReportGeriatrics and Gerontologybusinesshuman activities030217 neurology & neurosurgeryHearing.statusCohort studyJournal of the American Geriatrics Society
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Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deaf…

1993

Two sibs, whose parents are first cousins, had diabetes mellitus with hyperinsulinism, insensitive insulin receptors, and acanthosis nigricans. Both patients had pigmentary retinopathy, secondary cataracts, labyrinthine deafness, mental retardation, and cerebral atrophy. They were disproportionately short with relatively broad hands and feet and slightly coarse face. The young woman had secondary amenorrhea and polycystic ovaries and the boy gynecomastia and hypergonadotrophic hypogonadism. This appears to be the second family with a new autosomal recessive disorder differing from Alstrom syndrome by the presence of mental retardation and absence of renal insufficiency. Impaired insulin rec…

Malemedicine.medical_specialtyAdolescentHearing Loss SensorineuralGenes RecessiveConsanguinityInternal medicineDiabetes mellitusIntellectual DisabilityMedicineHumansAcanthosis NigricansAcanthosis nigricansGenetics (clinical)business.industryHypogonadismSyndromemedicine.diseasePolycystic ovaryEndocrinologyGynecomastiaDiabetes Mellitus Type 2Insulin receptor bindingFemaleInsulin ResistancebusinessHyperinsulinismRetinitis PigmentosaAlström syndromeRetinopathyPolycystic Ovary SyndromeAmerican journal of medical genetics
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Inner ear function in children with Fabry disease

2007

Aim: The prevalence of hearing loss in patients with Fabry disease is still uncertain. This paper examines hearing loss in a group of young patients with Fabry disease. Methods: A clinical ear nose and throat examination,pure-tone air and bone conduction audiometry, speech audiometry and middle ear testing (tympanometry and acoustic reflex testing) were carried out in four girls and two boys with Fabry disease (age, 7-17 years), receiving enzyme replacement therapy (ERT). Results: None of the patients complained of a hearing disorder or suffered from hearing loss. Three female patients reported tinnitus; however, this was not reported as being a problem. One boy reported tinnitus for the fi…

Malemedicine.medical_specialtyAdolescentHearing lossAudiologyTinnitusBone conductionotorhinolaryngologic diseasesmedicineHumansChildmedicine.diagnostic_testbusiness.industryGeneral MedicineEnzyme replacement therapyTympanometrymedicine.diseaseFabry diseaseHearing disorderPediatrics Perinatology and Child HealthFabry DiseaseFemalemedicine.symptomAudiometrybusinessTinnitusActa Paediatrica
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Cognitive skills in achondroplasia

1993

Increased intracranial pressure and ventricular and subarachnoidal dilatation are common manifestations in achondroplasia. They rarely lead to major neurologic and/or psychomotor deficits and neurosurgical intervention is seldom needed. The present study was undertaken to detect signs of minor cerebral dysfunction and discuss possibilities of their prevention. Thirty children with achondroplasia were compared to 3 control groups: their next-born sibs, 30 children with other forms of dwarfism, and 30 children with normal height. Early development was assessed by means of questionnaires. Cognitive skills were evaluated with the German version of the Cognitive Abilities Test and the Lorge-Thor…

Malemedicine.medical_specialtyAdolescentHearing lossHearing Loss ConductivePopulationDwarfismAudiologyAchondroplasiaCognitionmedicineHumansAchondroplasiaChildeducationGenetics (clinical)Psychomotor learningeducation.field_of_studybusiness.industrymedicine.diseaseNeuroticismHypotoniaChild PreschoolSpeech PerceptionAnxietyFemalemedicine.symptomCognition DisordersbusinessAmerican Journal of Medical Genetics
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