Dissertations / Theses on the topic 'Congenital sensorineural hearing loss'
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Strike, Brian J. "The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss." University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212164935.
Full textCahill, Lisa D. "Cortical responses to speech stimuli in hearing impaired infants measured by fMRI and auditory evoked potentials." University of Cincinnati / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1273174165.
Full textGeldenhuys, Wilhelmien. "The relationship between motor proficiency, bilateral vestibular hypofunction and dynamic visual acuity in children with congenital or early acquired sensorineural hearing loss." Master's thesis, University of Cape Town, 2010. http://hdl.handle.net/11427/10505.
Full textThe functional integrity of the vestibular system in children is not often tested. Due to the close relationship between the cochlea and the peripheral vestibular system, the function of the vestibular system may be impaired in children with sensorineural hearing loss.The aims of this study were to determine the prevalence of impairments of motor performance, vestibular function and dynamic visual acuity, and the nature and extent of interaction between these in children between the ages of four and fourteen years with congenital and early acquired sensorineural hearing loss. Motor performance was evaluated by means of the Movement Assessment Battery for Children-2, dynamic visual acuity was determined by means of the Dynamic Visual Acuity Test, and vestibular function with the Southern California Postrotary Nystagmus Test.
Silva, Adriana Carnevale da. "Infecção congênita por CMV: potenciais marcadores preditivos de alterações tardias em crianças assintomáticas." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/17/17144/tde-23032018-104745/.
Full textThe objectives of this study were to verify the impact of congenital cytomegalovirus (CMV) infection at birth and to evaluate potential prognostic predictors of late abnormalities in a cohort of children with this infection. Methods: By means of a CMV neonatal screening, 66 of 11.957 infants were identified as congenitally infected. Infants with and without clinical abnormalities detectable at birth underwent physical examination, cranial ultrasound performed by a paediatric radiologist and/or cranial magnetic resonance imaging, ocular fundoscopy, and hearing evaluation using evoked otoacoustic emissions and auditory brainstem response. Logistic regression analysis was carried out to verify the association between the risk factors for occurrence of hearing loss related to CMV and/ or abnormal cranial ultrasound findings. ROC curve was plotted using the log10 value of CMV DNA load to evaluate the association between viral load and clinical symptoms at birth, abnormal cranial ultrasound findings and hearing loss. Results: Of all 66 infected children, the clinical signs suggestive of congenital infection at birth were observed in 8/66 (12.12%; IC95%: 5.74- 23.03) symptomatic infants. Sensorineural hearing loss was observed in 8/66 (12,12%; IC95%: 5.74-23.03%) children. Of these, 4/58 (6,9%; IC95%: 2.23-17.54%) and 4/8 (50%; IC95%: 17,44-82.55%) children were asymptomatic and symptomatic, respectively. Cranial ultrasound findings suggestive of congenital infection were observed in 7 of the 8 symptomatic children (87.5%; IC95%: 46.67-99.34%). Among the 58 asymptomatic infants, 53 underwent complete evaluation and 29/52 had abnormal cranial ultrasound results (55,7%; IC95%: 41.41 - 69,27%). The most prevalent findings was lenticulostriate vasculopathy with subependymal pseudocysts present in 13 of the /29 (43.3%) infants with cranial ultrasound. Other abnormal findings were isolated subependymal pseudocysts (11/29: 37.9%); single or periventricular calcifications and/or gliosis (4/29: 13.8%); and ventriculomegaly (4/29: 13,8%). Logistic regression analysis showed that only the presence of clinical findings predicted the occurrence of hearing loss. Cranial ultrasound findings were observed in 3 of asymptomatic infants (75.0%) while 26 (54.2%) of 48 infants with no hearing loss had abnormal imaging features (p=0,42; RR:2,38: IC95%: 0,26-21,39). None of the other factors risk were independely associated with development of hearing loss. The presence of thrombocytopenia and/or high level of gamma-glutamyltranspeptidase (?GT) was associated with cranial ultrasound findings on univariated analysis. No discrimination power was achieved using the area under the ROC curve to verify the association between CMV DNA load in the urine of the infected children and the developing of hearing loss, presence of cranial ultrasound findings and clinical signs at birth. Conclusions: Although a neonatal screening of cCMV will identify the majority of infected infants who are clinically asymptomatic, a significant proportion of them could benefit from a central nervous system image evaluation, since abnormal findings are frequent. Althoug it was not possible to determine risk factors that are independently associated to development of sensorineural hearing loss, cranial ultrasound findings could be a potential prognostic markers of adverse outcomes of congenital CMV in asymptomatic infants.
Seeman, Scott E. "Informational Masking and Sensorineural Hearing Loss." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250704738.
Full textNakashima, T., T. Yoshida, S. Nakata, M. Teranishi, I. M. Ishida, S. Naganawa, and M. Sugiura. "Vestibular aqueduct in sudden sensorineural hearing loss." Cambridge University Press, 2008. http://hdl.handle.net/2237/14312.
Full textPizarro, Luzia Maria Pozzobom Ventura. "Maturação cortical e habilidades auditivas em usuários experientes de Vibrant Soundbridge: estudo eletrofisiológico e comportamental." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/5/5143/tde-27092018-084134/.
Full textIntroduction: Congenital aural atresia is a congenital deformity. It is unilaterally prevalent due to alterations in the development of the external and middle ear structures. Congenital aural atresia causes conductive hearing loss and can be accompanied by sensorineural component. Among the available forms of treatment is the middle ear implant, Vibrant Soundbridge (VSB), which has been shown to be effective in treating this type of alteration. The literature shows improvement in tonal thresholds and in the results of tests of auditory perception of speech that were performed using the speech processor after surgery. Individuals with this type of malformation often experience a period of auditory sensory deprivation prior to rehabilitation. Hence, it is important to evaluate the maturation stage of the cortical auditory structures, the processing of auditory information at the central level, and to verify the benefit of unilateral VSB in difficult listening situations. There are no previous data on this aspect and with the use of cortical auditory evoked potentials (CAEP) and event-related potential (P300) in users of VSB. Aim: To analyze the impact of conductive and mixed hearing loss on CAEP and P300 in unilateral VSB users with bilateral ear atresia. To verify the auditory abilities in a difficult listening situation considering the indication for unilateral VSB. Materials and methods: Twenty individuals were divided into two groups matched for age, sex, and educational level. G1 comprised ten individuals with bilateral conductive or mixed hearing loss and users of unilateral VSB, who visited the research institution. All subjects used conventional hearing aids prior to VSB. G2 comprised ten normal hearing individuals. Audiometry in the free field was performed with the use of VSB (G1 only) and evaluation of hearing skills by the Hearing in Noise Test was conducted; components P1, N1, P2, N2, and P300 in a calibrated field were recorded. Results: Evaluation of the mean tonal thresholds in the frequencies between 500 and 3000 Hz, from 20 to 36 dB HL, demonstrated that VSB allowed access to speech sounds. There was no statistically significant difference in the CAEP and P300 latency values between the two groups. A statistically significant difference was observed in the sentence recognition threshold and the signal-to-noise ratio between the groups, with best results presented by G2. Conclusion: Individuals with congenital aural atresia and bilateral conductive or mixed hearing loss may reach maturation of the central auditory pathway and achieve adequate processing of auditory information at the cortical level, when rehabilitated. The auditory recognition skills, with and without competitive noise, were shown to be out of phase with normality, indicating the need for a bilateral VSB
Graf, Isaac John 1972. "Simulation of the effects of sensorineural hearing loss." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/42761.
Full textIncludes bibliographical references (leaves 103-112).
by Isaac John Graf.
M.S.
Cullen, J. R. "Sudden hearing loss : an animal model." Thesis, Queen's University Belfast, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326426.
Full textJohnson, Earl E. "Amplification Options for Severe-to-Profound Sensorineural Hearing Loss." Digital Commons @ East Tennessee State University, 2014. https://dc.etsu.edu/etsu-works/1974.
Full textWilson, Richard H., Robert King, and Faith W. Akin. "Unilateral Transitory Sensorineural Hearing Loss Following a Dental Procedure." Digital Commons @ East Tennessee State University, 2009. https://dc.etsu.edu/etsu-works/2423.
Full textMujica, Mota Mario. "Otoprotection of metformin in radiation-induced sensorineural hearing loss." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=117200.
Full textIntroduction: La radiothérapie peut provoquer une perte auditive permanente quand l'oreille est incluse dans la zone de radiation. Il n'y existe aucun traitement préventif pour cet effet néfaste. La radiation provoque la formation des radicales libres entrainant la mort de cellules dans l'organe de Corti. La Metformine, un médicament vastement utilisé dans le traitement du diabète a montré des propriétés anticancéreuses et antivieillissement par la régulation de la production d'espèces réactives de l'oxygène après le stress cellulaire. Objectifs: Déterminer l'ototoxicité et les propriétés radio-protectives de la Metformine contre l'atteinte cochléaire provoqué par radiation in vivo et in vitro.Matériaux et méthodes: Les cellules auditives cultivées (HEI-OC1) ont été exposées à différentes concentrations de Metformine pour déterminer le potentiel d'ototoxicité de ce dernier. En plus, les cellules ont été incubées avec diverses concentrations et par la suite, exposées à la radiation. La survie cellulaire a été déterminée par la méthode MTS. Quinze cochon d'Inde ont été divisés en deux groupes: buvant de l'eau potable (n=7) et buvant de l'eau contenant la Metformine (n=8) avec une dose de 100 mg /kg/jour. Les oreilles des animaux ont été irradiées unilatéralement pendant 20 jours (dose totale 71 Gy) et par conséquence ont été divisées en quatre groupes: Control (n=7), Irradiées (n=7), Metformine (n=8), Expérimentales (n=8). Les Produits de Distorsion des Émissions Otoacoustiques (PDEO) et les Réponses Auditives du Tronc Cérébral (RATC) ont été six semaines après la radiothérapie.Résultats: La Metformine n'est pas été ototoxique ou radio-protective des cellules auditives cultivées. Les PDEO test n'ont pas montré de perte auditive ou de différences entre les quatre groupes aux différents temps évaluées. Après six semaines. Les oreilles expérimentales ont eu moins de perte auditive comparées aux oreilles irradiées, néanmoins les différences n'ont pas été significatives.Conclusion: La Metformine n'est pas ototoxique in vitro ou in vivo. La Metformine n'a pas été otoprotective in vitro ou contre la perte auditive causée par radiation après un suivi de six semaines après la fin de la radiothérapie.
Johnson, Earl E. "Fitting a Hearing Aid to Conductive Hearing Loss and Realistic Expectations When Fitting a Hearing Aid to Sensorineural Hearing Loss." Digital Commons @ East Tennessee State University, 2013. https://dc.etsu.edu/etsu-works/1740.
Full textEager, Katrise Mary. "Rehabilitation of unilateral profound sensorineural hearing loss with a bone anchored hearing aid." University of Western Australia. School of Surgery, 2010. http://theses.library.uwa.edu.au/adt-WU2010.0061.
Full textSchairer, Kim, Douglas H. Keefe, Denis Fitzpatrick, Daniel Putterman, Elizabeth Kolberg, Angie Garinis, Michael Kurth, Kara McGregor, Ashley Light, and M. P. Feeney. "Wideband Transient Otoacoustic Emissions in Ears with Normal Hearing and Sensorineural Hearing Loss." Digital Commons @ East Tennessee State University, 2018. https://doi.org/10.1121/1.5068081.
Full textWilding, Phillipa Jane. "Speech Understanding Abilities of Older Adults with Sensorineural Hearing Loss." Thesis, University of Canterbury. Department of Communication Disorders, 2010. http://hdl.handle.net/10092/4473.
Full textArioz, Umut. "Developing Subject-specific Frequency Lowering Algorithms With Simulated Hearing Loss For The Enhancement Of Sensorineural Hearing Loss." Phd thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614929/index.pdf.
Full textPereira, Sónia Lopes. "Sudden sensorineural hearing loss : evaluation of co-morbidities and potential clinical associations." Master's thesis, Faculdade de Ciências Médicas, 2013. http://hdl.handle.net/10362/10862.
Full textOosthuizen, Ilze. "Listening effort in children with severe-profound sensorineural unilateral hearing loss." Thesis, University of Pretoria, 2021. http://hdl.handle.net/2263/78542.
Full textThesis (PhD (Audiology))--University of Pretoria, 2020.
This research project was funded by Sonova,AG.
Speech-Language Pathology and Audiology
PhD (Audiology)
Unrestricted
Ballantyne, Deborah. "An algorithm for the fitting of hearing aids." Thesis, University of Southampton, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318218.
Full textOlsen, Henrik L. "Supra-threshold hearing loss and wide dynamic range compression /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7349-921-8.
Full textNosrati-Zarenoe, Ramesh. "Idiopathic Sudden Sensorineural Hearing Loss : Corticosteroid Treatment, the Diagnostic Protocol and Outcome." Doctoral thesis, Linköpings universitet, Oto-Rhino-Laryngologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-67609.
Full textMillward, Kerri E. "Consequences of mild sensorineural hearing loss for listening and learning in children." Thesis, University of Nottingham, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523608.
Full textSmurzynski, Jacek, Krzysztof Kochanek, Adam Pilka, and Henryk Skarzynski. "Distortion-product Otoacoustic Emissions in Patients with Low-frequency Sensorineural Hearing Loss." Digital Commons @ East Tennessee State University, 2007. https://dc.etsu.edu/etsu-works/2194.
Full textZarenoe, Reza. "Tinnitus in Patients with Sensorineural Hearing Loss : Management and Quality of Life." Licentiate thesis, Linköpings universitet, Institutionen för klinisk och experimentell medicin, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-81413.
Full textGiovanni, Monica A. "A Family-Based Mapping Study of Autosomal Dominant Nonsyndromic Sensorineural Hearing Loss." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179241536.
Full textMallick, Ali Sameer. "Stem cell therapies for sensorineural hearing loss : understanding the role of glial cells." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/19788/.
Full textJONAS, CATHERINE EILEEN. "CHARACTERISTICS OF AUDITORY PROCESSING ABILITIES AND UNILATERAL SENSORINEURAL HEARING LOSS: A PILOT STUDY." University of Cincinnati / OhioLINK, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1022687699.
Full textDinsman, Patricia L. "Social/emotional problems among children and youth with differing degrees of sensorineural hearing loss." CSUSB ScholarWorks, 1991. https://scholarworks.lib.csusb.edu/etd-project/738.
Full textPotgieter, Jenni-Marí. "An Auditory profile of sclerosteosis." Diss., University of Pretoria, 2013. http://hdl.handle.net/2263/33363.
Full textDissertation (MCommunication Pathology)--University of Pretoria, 2013.
gm2014
Speech-Language Pathology and Audiology
Unrestricted
Zarenoe, Reza. "Tinnitus in Patients with Sensorineural Hearing Loss : Management, Quality of Life and Treatment Strategies." Doctoral thesis, Linköpings universitet, Avdelningen för neuro- och inflammationsvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-132163.
Full textNosrati-Zarenoe, Ramesh. "Idiopathic Sudden Sensorineural Hearing Loss in Sweden : Diagnostic Protocol and Treatment in Relation to Outcome." Licentiate thesis, Linköping University, Linköping University, Oto-Rhiono-Laryngology and Head & Neck Surgery, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-19023.
Full textIdiopathic Sudden Sensorineural Hearing Loss (ISSNHL) is a rapid loss of hearing caused by damage to the cochlea (inner ear) or auditory nerve. Spontaneous recovery has been seen in 32% - 81%. The incidence of the ISSNHL has been estimated to be between 5 and 20 per 100,000 per year. Different theories (infections, vascular catastrophes, immunologic damage or intracochlear membrane break) about the etiology have resulted in different treatment policies. The effect of therapy is difficult to evaluate for a single physician who sees just a few patients annually.
The aim of the present thesis was to analyze the management and treatment of ISSNHL patients in Sweden with regard to outcome.
A national database was developed for Sweden with half of all ENT clinics in Sweden participating by submitting a questionnaire for each patient with SSNHL. The questionnaire covered the patient’s background, current disorder, past and family history of different diseases, examinations and treatment. Audiograms at the onset of SSNHL and after three months were requested.
All results were analyzed using ordinal logistic regression looking for interactions with hearing recovery and remaining hearing loss as dependent variables. Independent of treatment or no therapy heredity for hearing loss (I, II), older age (I, II) and presence of vertigo (II) was significantly associated with negative outcome. 40% of all patients had an MRI or CT, where 3 – 4% had acoustic neuroma. 24% of patients with ISSNHL who had hematological tests taken had one or more pathological findings. Blood screening varied from simple routine tests to a complete analysis with such tests as HSP70, Anti-Neutrophilic Cytoplasmic Antibodies (ANCA) and Borrelia tests. There was no association between any of these laboratory tests and either hearing improvement or remaining hearing loss evaluating the tests separately (I, II) or after categorization in comparison with those who had normal laboratory findings (II). Patients with hearing loss in the mid-frequency region had significantly better odds for hearing improvement compared to the other three frequency regions (low, high and “flat loss”). Almost 60% of patients with ISSNHL were medically treated, of which nearly 90% got corticosteroids. The medication had no association with either hearing improvement or remaining hearing loss. However, patients who were prescribed rest or sick leave had higher odds for hearing improvement regardless of other treatment. Those patients who did not receive any treatment at all also came significantly later to the ENT clinics than those treated medically and consequently had worse prognosis.
Conclusion: There is no standard program for management or treatment of ISSNHL in Sweden. The diagnostic protocol varies. MRI is an underused resource to get specific diagnoses for the condition especially acoustic neuromas. Regardless of pathological findings, treatment is mainly limited to corticosteroids or no medication with no difference in outcome. A randomized placebo controlled study is necessary to evaluate whether there is an effect of corticosteroids on ISSNHL.
Grobbelaar, Annerina. "Linear frequency transposition and word recognition abilities of children with moderate-to-severe sensorineural hearing loss." Diss., Pretoria : [s. n.], 2009. http://upetd.up.ac.za/thesis/available/etd-03112010-104801.
Full textLehtonen, M. (Mervi). "Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish population." Doctoral thesis, University of Oulu, 2002. http://urn.fi/urn:isbn:9514268490.
Full textSpirakis, Susan E. "Incidence of Unilateral, High Frequency, Sensorineural Hearing Loss in Shunt Treated Hydrocephalic Children Ipsilateral to Shunt Placement." Scholar Commons, 2000. https://scholarcommons.usf.edu/etd/1548.
Full textMuller, Claudia. "Extended frequency amplification, speech recognition and functional performance in children with mild to severe sensorineural hearing loss." Diss., University of Pretoria, 2012. http://hdl.handle.net/2263/30077.
Full textDissertation (MCommunication Pathology)--University of Pretoria, 2012.
Speech-Language Pathology and Audiology
Unrestricted
Mondelli, Maria Fernanda Capoani Garcia. "Desempenho de crianças com perda auditiva leve no teste da habilidade de atenção auditiva sustentada - THAAS." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/61/61131/tde-12112007-145751/.
Full textObjective: To verify the performance of children diagnosed with a hearing loss of mild degree, conductive and sensorineural, at Sustained Auditory Attention Ability Test (SAAAT), aiming to observe if this test suffers the influence of the presence of a hearing loss. Model: A study of the Sustained Auditory Attention Ability Test ? SAAAT in three groups: group 1 (G1) control group comprising children with normal hearing, group 2 (G2) children with a bilateral sensorineural hearing loss of a mild degree and group 3 (G3), comprising children with a bilateral conductive hearing loss of a mild degree. Place: Division for Hearing Health ? Craniofacial Anomaly Rehabilitation Hospita, University of São Paulo (HRAC/USP). Participants: 7 to 11 year old children, 30 for each group. Interventions: Pure Tone Audiometry, Immitance Acoustic and SAAAT. Results: There were not any statistically significant indications between sex and age in all studied groups. Sensorineural and conductive groups showed a lower performance related to control group in all answers for SAAAT. Conclusions: SAAAT test suffered the influence of conductive and sensorineural hearing losses of light degree in studied population, the worse compromise occurring for sensorineural losses.
Kritzinger, Mieke. "Cortical Auditory Evoked Potential (CAEP) and the chirp Auditory Steady State Response (ASSR) in predicting behavioural hearing thresholds in adults with sensorineural hearing loss." Diss., University of Pretoria, 2019. http://hdl.handle.net/2263/73231.
Full textDissertation (MA (Audiology))--University of Pretoria, 2019.
Speech-Language Pathology and Audiology
MA Audiology
Unrestricted
Saremi, Amin G. "Effects of Specific Cochlear Pathologies on the Auditory Functions : Modelling, Simulations and Clinical Implications." Doctoral thesis, Linköpings universitet, Avdelningen för neurovetenskap, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-105810.
Full textBacsfalvi, Penelope Cindy Emese. "Visual feedback technology with a focus on ultrasound : the effects of speech habilitation for adolescents with sensorineural hearing loss." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/31208.
Full textMedicine, Faculty of
Audiology and Speech Sciences, School of
Graduate
Szeto, Mei-Wa Tam. "Effects of age and hearing loss on perception of dynamic speech cues." [Tampa, Fla] : University of South Florida, 2008. http://purl.fcla.edu/usf/dc/et/SFE0002732.
Full textHällgren, Mathias. "Hearing and cognition in speech comprehension : methods and applications /." Linköping : Univ, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-5039.
Full textOlive, Darlene W. "Association Between Smoking, Chemical Exposure and Hearing Loss in an Occupational Setting." VCU Scholars Compass, 2006. http://hdl.handle.net/10156/1920.
Full textLinares, Ana Emília. "Correlação do potencial evocado auditivo de estado estável com outros achados em audiologia pediátrica." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-25022010-142312/.
Full textIntroduction: The mainly question regarding pediatric audiolological diagnosis is determining procedures to configure reliable results and objectives, which can be use to predict hearing thresholds by frequencyspecifics. Objective: The purpose of this study was to study the correlation between auditory steady-state response (ASSR) with other exams in children with sensorineural hearing loss. Methods: Twenty-three children (age 1 to 7; mean, 3 yr) were submitted to ASSR, behavioral audiometry, click audiometry brain stem response (ABR), tone burst ABR, and predicting hearing level from the acoustic reflex. Results: the correlation between behavioral thresholds and ASSR was (0.70- 0.93), for the ABR tone burst it was (0.73 -0.93), for the ABR click it was (0.83-0.89) only at 2k and 4kHz. The conformity between the hearing loss degree the ASSR and acoustical reflex was moderate. Conclusion: There was significant correlation between ASSR, behavioral audiometry, click ABR only for 2k and 4kHz, tone burst ABR. The acoustic reflex can be use to add accuracy in the infant diagnosis
Carvalho, Marcelo Alexandre. "Estudo funcional das vias auditivas perifÃricas e centrais em pacientes com acromegalia." Universidade Federal do CearÃ, 2012. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=9341.
Full textAcromegaly is a rare endocrine disease. Few studies have evaluated its association with hearing loss (HL) or disturbance in conduction of the auditory neural impulse. The results are conflicting. The aim is to evaluate central and peripheral auditory transmission in acromegalic patients. Besides, to evaluate the prevalence and characteristics of HL in patients with acromegaly. A cross-sectional study was carried out on 36 patients with acromegaly in a specialized ambulatory in Fortaleza-CearÃ. Patients with abnormal otoscopy, family history of hearing loss, use of ototoxic drugs or occupational noise exposure were excluded. Initially, the group was evaluated by pure tone audiometry. HL was considered when pure tone average was > 25 DBHL for low frequencies (250, 500, 1000 e 2000 Hz) or high frequencies (3000, 4000, 6000 e 8000 Hz). The whole group was divided in: acromegaly with HL (Acro HL) and without HL (AcroNHL) and compared in regards to hormonal levels and metabolic parameters. Additionally that group of patients with acromegaly was divided into 2 subgroups: with (n=16) and without (n=20) diabetes mellitus/impaired glucose tolerance (DM/IGT). The results were compared among these subgroups and a control group (n=20) regarding the brainstem auditory evoked potentials (BAEP) parameters.Kolmogorov-Smirnov test was used to evaluate the normality of distribution when necessary. Qui-quadrado, Student t test and Pearson correlation coefficient were carried out. The level of statistical significance chosen was at p<0.05 (statistical package for social sciences-SPSS 12.0). Among 36 patients evaluated, 14 (38,9%) showed sensorioneural HL (Acro HL), being 9 bilateral and 5 unilateral cases. No one had mixed or conductive HL. The prevalence of diabetes/impaired glucose tolerance was similar between the groups. The frequencies 250, 3000, 4000, 6000 and 8000 Hz were the most affected and with a similar pattern in both ears. The group with acromegaly showed a prolonged peak I latency in the right ear in comparison to the control group (p=0,007), with no difference regarding the interpeak intervals in any sides. This pattern was the same when comparing the DM/IGT subgroup to controls. Also, we found a prolonged peak I latency in the right ear in relation to the left ear in the group with acromegaly.In conclusion, a high prevalence of sensorineural HL was shown in patients with acromegaly. Nevertheless, no correlation was observed between this dysfunction and clinical or metabolic characteristics of the disease. Patients with acromegaly associated with DM/IGT showed a delayed neural impulse in the auditory nerve unilaterally in the right side, evidencing a non-homogenous neuropathic effect of the carbohydrate metabolism disturbances on the auditory nerve.
Van, Dyk Zandri. "Diagnostic accuracy of CE Chirp." Diss., University of Pretoria, 2019. http://hdl.handle.net/2263/72463.
Full textDissertation (MA Audiology) University of Pretoria, 2019.
Speech-Language Pathology and Audiology
MA (Audiology)
Unrestricted
Halliday, Lorna F. "Are auditory processing deficits linked to literacy problems : a comparison of specific reading disability and mild to moderate sensorineural hearing loss." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.427616.
Full textHällgren, Mathias. "Hearing and cognition in speech comprehension. Methods and applications." Doctoral thesis, Linköpings universitet, Teknisk audiologi, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-5039.
Full textThe ISBN 91-85297-49-6 in the printed verison is incorrect. The correct ISBN is 91-85297-93-3.
Tan, Lirong. "Identification of Disease Biomarkers from Brain fMRI Data using Machine Learning Techniques: Applications in Sensorineural Hearing Loss and Attention Deficit Hyperactivity Disorder." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1447689755.
Full textKenworthy, Maura Koenig. "An Examination of the Relationship Between the U-Titer II and Hearing Aid Benefit." Scholar Commons, 2002. https://scholarcommons.usf.edu/etd/1522.
Full text