Search results for " Hearing"

showing 10 items of 301 documents

Neonatal Hearing Screening: Three years of experience in Western Sicily

2006

Neonatal Hearing ScreeningSettore MED/31 - OtorinolaringoiatriaSettore MED/32 - Audiologia
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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
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Genetic determinants of ototoxicity during and after childhood cancer treatment: Protocol for the pancarelife study

2019

BACKGROUND: Survival rates after childhood cancer now reach nearly 80% in developed countries. However, treatments that lead to survival and cure can cause serious adverse effects with lifelong negative impacts on survivor quality of life. Hearing impairment is a common adverse effect in children treated with cisplatin-based chemotherapy or cranial radiotherapy. Ototoxicity can extend from high-tone hearing impairment to involvement of speech frequencies. Hearing impairment can impede speech and language and neurocognitive development. Although treatment-related risk factors for hearing loss following childhood cancer treatment have been identified, the individual variability in toxicity of…

OncologyCandidate gene020205 medical informaticscisplatinCHILDREN02 engineering and technologyVARIANTSPLATINUM-INDUCED OTOTOXICITYChildhood cancer survivors0302 clinical medicineTPMT0202 electrical engineering electronic engineering information engineeringProtocolGWASgenetics030212 general & internal medicineSURVIVORSGeneral MedicineCHEMOTHERAPY3. Good healthototoxicityCohortmedicine.symptomcandidate genes020 Library & information sciencesmedicine.medical_specialtyINDUCED HEARING-LOSSHearing losschildhood cancer survivors610 Medicine & healthINTERNATIONAL SOCIETYCandidate genes03 medical and health sciencesACYP2OtotoxicitySDG 3 - Good Health and Well-being360 Social problems & social servicesInternal medicinemedicineGenetic predispositionGeneticsCISPLATIN-INDUCED OTOTOXICITYAdverse effecthearing lossbusiness.industryCancerHearing lossmedicine.diseaseOtotoxicityClinical trialCisplatinbusinessPolymorphismspolymorphisms
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SAT0513 Brainstem Auditory Evoked Potentials and Visual Potentials in Kawasaki Disease: Expression of CNS Vasculitis?

2015

Background Kawasaki disease (KD) is an acute, self-limited vasculitis of infants and children that is nowadays the most common cause of acquired heart disease in children. Transient sensorineural hearing loss (20 to 35 dB) is a possible complication of acute phase KD and may be related to salicylate toxicity in some patients. Objectives Brainstem Auditory Evoked Potentials (BAEPs) , and Visual Evoked Potentials (VEPs) were examined in 43 children (age: 0,8-7,5 years) affected by KD. No risk factors for hearing loss and/or neurological impairment of CNS were identified in all the patients. BAEPs showed altered waves II to V, in 18 patients (42%). Among these, in 4 patients (20%) VEPs showed …

Pathologymedicine.medical_specialtygenetic structuresHeart diseasebusiness.industryHearing lossImmunologyThalamusmedicine.diseaseGeneral Biochemistry Genetics and Molecular BiologyLesionRheumatologymedicineImmunology and AllergyKawasaki diseaseSensorineural hearing lossmedicine.symptombusinessVasculitisComplicationAnnals of the Rheumatic Diseases
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Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.

2009

We present the postnatal diagnosis of a de novo der(18)t(18;22)(p11.32;q11.21)pat, resulting in an unbalanced 45,XX,der (18)t(18;22) karyotype in a girl with conductive hearing loss on the left and ptosis of the right upper eye-lid. Unilateral ptosis was also observed in the patient’s 2 years and 8 months younger sister, who grows noticeably faster and appears to be a much quicker learner. After speech therapy the patient was eventually placed in normal school. The haploinsufficient 16.4-Mb region on chromosome 22pter→q11.21 contains 10 genes as well as many predicted genes, pseudogenes, and retrotransposed sequences with unknown functions. This observation may prove useful for prenatal dia…

Pathologymedicine.medical_specialtymedia_common.quotation_subjectChromosomes Human Pair 22BiologyHearing Loss UnilateralGeneticsmedicineHumansSpeechGirlMolecular BiologyGenetics (clinical)media_commonGeneticsInfant NewbornChromosomeKaryotypemedicine.diseaseConductive hearing lossHaplotypesKaryotypingFemaleUnilateral conductive hearing lossHaploinsufficiencyChromosomes Human Pair 18Chromosome 22Cytogenetic and genome research
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Prevalence of Hearing Impairment Among High-Risk Newborns in Ibadan, Nigeria

2018

The burden of severe hearing impairment is increasing with two-thirds of these hearing impaired people residing in developing countries. Newborn hearing screening helps to identify early, babies who need intervention in order to prevent future disability. Neither universal nor targeted hearing screening programme is available in Nigeria. Objectives: This study was carried out to assess the prevalence of hearing impairment among high-risk newborns in UCH and the associated risk factors. Materials and Methods: Two hundred one newborns in the neonatal unit of UCH with risk factors for hearing impairment had hearing screening done using automated auditory brainstem response (AABR) at 30, 45, an…

Pediatricsmedicine.medical_specialtyHearing lossNigeriaPediatricsHearing screeningsensorineural hearing loss03 medical and health sciences0302 clinical medicine030225 pediatricsmedicineotorhinolaryngologic diseases030223 otorhinolaryngologyOriginal Researchhigh-risk newbornbusiness.industrylcsh:RJ1-570auditory brainstem response (ABR)lcsh:Pediatricshearing impairmentmedicine.diseaseBilirubin encephalopathyPerinatal asphyxiaAmikacinPediatrics Perinatology and Child HealthSensorineural hearing lossmedicine.symptombusinessComplicationMeningitismedicine.drugFrontiers in Pediatrics
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Essential of audiology: screening and postscreening

2014

Newborn hearing screening is a type of screening testfor the early detection of hearing loss. It can recognizewith good accuracy newborns affected by hearingimpairment allowing an early diagnosis and interventionand avoiding cognitive and linguistic deficits [1-6].The incidence of bilateral sensorineural hearing loss(SNHL) in Sicily is 2.35 cases per 1000 newborns; thisvalue increases to 2.95 if we consider also unilateral SNHL[2,3] and to 10 cases per 1000 births among infants at risk[7-9].A correct newborn hearing screening programme isbased on different protocols depending on the presence/absence of audiologic risk factors:† Newborns without risk factors: [1-3]Initial Hearing Screening (…

Pediatricsmedicine.medical_specialtyRespiratory distressHearing lossbusiness.industryIncidence (epidemiology)Early detectionAudiologymedicine.diseaseHearing screeningSettore MED/32 - AudiologiaAuditory brainstem responseSettore MED/31 - OtorinolaringoiatriaSettore MED/38 - Pediatria Generale E SpecialisticaAuditory neuropathy spectrum disorderMeeting Abstractotorhinolaryngologic diseasesmedicineOTOFNeonatal hearing screeningmedicine.symptombusiness
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Therapy Strategies for Usher Syndrome Type 1C in the Retina

2014

The Usher syndrome (USH) is the most common form of inherited deaf-blindness with a prevalence of ~ 1/6,000. Three clinical subtypes (USH1–USH3) are defined according to the severity of the hearing impairment, the presence or absence of vestibular dysfunction and the age of onset of retinitis pigmentosa (RP). USH1 is the most severe subtype with congenital severe to profound hearing loss and onset of RP before puberty. Currently only the amelioration of the hearing deficiency is implemented, but no treatment of the senso-neuronal degeneration in the eye exists.

Pediatricsmedicine.medical_specialtyRetinabusiness.industryUsher syndromemacromolecular substancesDegeneration (medical)medicine.diseaseProfound hearing lossmedicine.anatomical_structurenervous systemRetinitis pigmentosaotorhinolaryngologic diseasesmedicineDeaf blindnessVestibular dysfunctionAge of onsetbusiness
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La educación auditiva como eje vertebrador de la educación musical en la Educación Secundaria Obligatoria

2013

El presente trabajo se enmarca dentro de un estudio de mayores dimensiones motivado por el interés de los autores en la didáctica de la audición musical, convencidos de que los principios fundamentales sobre los que se debería apoyar la educación musical actualmente en la Educación Secundaria Obligatoria son, por una parte, la necesidad de una mayor contribución de la misma a una educación integradora de todas las dimensiones del ser humano, y por otra, la conveniencia de otorgarle un mayor protagonismo a la educación auditiva en el proceso de enseñanza-aprendizaje de la materia de música en dicha etapa educativa. El propósito es dar respuesta a una serie de interrogantes que surgen en torn…

Percepció de la músicaRange (music)Secondary educationDidactical of musical hearingProcess (engineering)Musical educationIntegral educationEducación integralMusicalPercepció auditivaObject (philosophy)Educació secundària obligatòriaPedagogyConvictionPercepción musicalAction researchDidáctica de la audición musicalPsychologyMusical perceptionMúsica EnsenyamentESPIRAL. CUADERNOS DEL PROFESORADO
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Early signs of dyslexia from the speech and language processing of children

2009

The Jyvaskyla Longitudinal Study of Dyslexia project (JLD) has followed the development of 200 children from birth until 10 years of age. Half the children are from families in which at least one of the parents has dyslexia, thus the child has a high risk of becoming dyslexic, and half have no such risk. Here the main findings of four studies in linguistics from the JLD project are reviewed. The speech processing skills were studied in 6, 18, 24 and 30-month-old children. The findings show that early signs of dyslexia can be detected in speech processing both phonologically and morphosyntactically. These precursors can be seen in perception or production of duration, in the prosody and phon…

PhonotacticsResearch and Theorymedia_common.quotation_subjectDyslexiaLPN and LVNmedicine.diseaseSpeech processingBiological theories of dyslexiaLanguage and LinguisticsLinguisticsDevelopmental psychologySpeech and HearingOtorhinolaryngologyReading (process)medicineLearning to readProsodyPsychologySurface dyslexiamedia_commonInternational Journal of Speech-Language Pathology
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