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Relevant bibliographies by topics / Progressive hearing loss

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Academic literature on the topic 'Progressive hearing loss'

Author: Grafiati

Published: 25 May 2024

Last updated: 31 July 2025

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Journal articles on the topic "Progressive hearing loss"

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Hayes, Deborah, and Susan Dreith. "Catastrophic Progressive Hearing Loss in Childhood." Journal of the American Academy of Audiology 11, no. 06 (2000): 300–308. http://dx.doi.org/10.1055/s-0042-1748058.

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AbstractWe present a report on a 5-year-old child with a complex medical and audiologic history who exhibited catastrophic progression in hearing loss. Hearing loss was initially attributed to bacterial meningitis at age 3 months; progression was apparently related to perilymph fistula at age 8 years. Etiologies associated with progressive hearing loss in children as well as signs of progression and monitoring protocols for children at risk for progressive hearing loss are discussed. Abbreviations: ABR = auditory brainstem response, CMV = cytomegalovirus, JCIH = Joint Committee on Infant Heari

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Fitzpatrick, Elizabeth M., Flora Nassrallah, Bénédicte Vos, JoAnne Whittingham, and Jessica Fitzpatrick. "Progressive Hearing Loss in Children With Mild Bilateral Hearing Loss." Language, Speech, and Hearing Services in Schools 51, no. 1 (2020): 5–16. http://dx.doi.org/10.1044/2019_lshss-ochl-19-0013.

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Purpose This study investigated progressive hearing loss in a cohort of children who were identified with permanent mild bilateral hearing loss. Method This population-based study included 207 children with permanent mild bilateral hearing loss, diagnosed and followed from 2003 to 2016 in 1 region of Canada. Clinical characteristics and initial audiologic results were collected prospectively at diagnosis, and audiologic information was updated. Changes in hearing levels between the 1st and most recent assessment were analyzed to determine progressive hearing loss. Clinical characteristics were

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Vrabec, Jeffrey T. "Hydrocodone Use and Sensorineural Hearing Loss." Pain Physician 3;10, no. 5;3 (2007): 467–72. http://dx.doi.org/10.36076/ppj.2007/10/467.

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Background: The hydrocodone/acetaminophen combination is one of the most commonly used analgesic preparations. Isolated incidences of suspected association between hydrocodone abuse and rapidly progressive hearing loss have been reported. In this study, we describe the clinical characteristics of 5 patients presenting with progressive hearing loss and a history of hydrocodone use. Methods: Patients presenting with rapidly progressive bilateral hearing loss who had a documented history of hydrocodone use were selected for the study. The presentation, audiologic findings, associated comorbiditie

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Roberts, Deanne M., Matthew L. Bush, and Raleigh O. Jones. "Adult Progressive Sensorineural Hearing Loss." Otology & Neurotology 35, no. 2 (2014): 241–45. http://dx.doi.org/10.1097/mao.0b013e3182a437b3.

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Whelan, Alison, and Anne Hing. "Genetics of Progressive Hearing Loss." Seminars in Hearing 16, no. 03 (1995): 246–56. http://dx.doi.org/10.1055/s-0028-1083722.

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Levi, Haya, Lilly Tell, and Moshe Feinmesser. "Progressive Hearing Loss in Hard-of-Hearing Children." International Journal of Audiology 32, no. 2 (1993): 132–36. http://dx.doi.org/10.3109/00206099309071862.

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de Wolf, M. J. F., J. Honings, F. B. M. Joosten, L. Hoefsloot, E. A. M. Mylanus, and C. W. R. J. Cremers. "Two siblings with progressive, fluctuating hearing loss after head trauma, treated with cochlear implantation." Journal of Laryngology & Otology 124, no. 1 (2009): 86–89. http://dx.doi.org/10.1017/s0022215109990296.

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AbstractObjective:Description of two siblings with unexplained, progressive, perceptive hearing loss after head trauma.Design:Case report.Subjects:Two siblings aged six and eight years old with bilateral, intermittent but progressive hearing loss.Results:These patients had a c.1172G>A (p.Ser391Asn) mutation in the SLC26A4 gene, which has not previously been reported and which caused Pendred or enlarged vestibular aqueduct syndrome. The diagnosis was based on the perceptive hearing loss, computed tomography findings and mutation analysis. The patients were each fitted with a cochlear implant

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Reisser, Christoph F. V., William J. Kimberling, and Christian R. Otterstedde. "Hearing Loss in Usher Syndrome Type II is Nonprogressive." Annals of Otology, Rhinology & Laryngology 111, no. 12 (2002): 1108–11. http://dx.doi.org/10.1177/000348940211101208.

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Usher syndrome is an autosomal recessive disorder characterized by sensorineural hearing loss and progressive visual loss secondary to retinitis pigmentosa. In the literature, a possible progression of the moderate to severe hearing loss in Usher syndrome type II (Usher II) is controversial. We studied the development of the hearing loss of 125 patients with a clinical diagnosis of Usher syndrome type II intraindividually and interindividually by repeatedly performing complete audiological and neuro-otologic examinations. Our data show a very characteristic slope of the hearing curve in all Us

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Lahiri, Asish Kumar, Anandita Gupta, Rakesh Vohra, Shalabh Sharma, and Satinder Singh. "Cochlear Otosclerosis: An Undiagnosed Cause of Progressive Sensorineural Hearing Loss." Bengal Journal of Otolaryngology and Head Neck Surgery 28, no. 2 (2020): 127–37. http://dx.doi.org/10.47210/bjohns.2020.v28i2.329.

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Introduction Otosclerosis presents as conductive or mixed hearing loss depending upon the stage of the disease. Isolated sensorineural hearing loss though known to occur has been rarely reported. Pure cochlear otosclerosis presenting as sensorineural hearing loss should be considered as a differential diagnosis in young patients presenting with progressive hearing loss. The aim of this article is to note the prevalence of cochlear otosclerosis in young patients presenting with progressive sensorineural hearing loss.  Materials and Methods Retrospective chart analysis of 19 pa

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Hashimoto, Sho, and Harold F. Schuknecht. "Progressive Hearing Loss from Strial Dysplasia." Annals of Otology, Rhinology & Laryngology 96, no. 2 (1987): 229–31. http://dx.doi.org/10.1177/000348948709600219.

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An otherwise healthy male patient had a bilateral, slowly progressive hearing loss first noticed in early childhood and possibly present at birth. Audiometric studies at the age of 32 showed a moderately severe, bilateral, mixed type hearing loss. He died of unrelated causes at the age of 34. Studies of the temporal bones showed bilateral hypoplasia and atrophy of the striae vascularis as the cause of hearing loss. The history and findings are consistent with a genetically determined hypoplasia and atrophy of this structure.

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Dissertations / Theses on the topic "Progressive hearing loss"

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Hilton, Jennifer Maglona. "Progressive hearing loss in mouse mutants." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610680.

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Light, Katrina Jane. "Reactions and Responses to the Diagnosis of a Progressive Hearing Loss in Adults." Thesis, University of Canterbury. Communication Disorders, 2009. http://hdl.handle.net/10092/3614.

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Being given the diagnosis of a disability generally affects an individual's emotional state, however, this has not previously been investigated with respect to audiology and the diagnosis of hearing loss. The first aim of this study was to describe some of the common initial reactions to the diagnosis of hearing loss (HL). An awareness of these emotional reactions will aid audiologists in counselling their patients. Counselling occurs at the time of the diagnosis and throughout the aural rehabilitation process. However, counselling tuition is currently not provided for audiology students at Ne

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Wentling, Maureen. "Characterization of the disease mechanisms underlying clarin-mediated progressive hearing loss." Electronic Thesis or Diss., Sorbonne université, 2023. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2023SORUS386.pdf.

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Malgré la forte prévalence de la déficience auditive, les mécanismes sous-jacents de la perte auditive progressive restent inconnus. Notre laboratoire a étudié le(s) rôle(s) de la clarine-1, responsable du syndrome d'Usher de type III, qui entraîne une perte auditive progressive, et de la clarine-2, responsable de la surdité non syndromique, dans le système auditif. En raison de la variabilité phénotypique chez les patients atteints du syndrome d'Usher de type III, même parmi les patients présentant les mêmes mutations génétiques, nous avons émis l'hypothèse qu'il pourrait y avoir une redondan

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Rönnåsen, Berit. "Aspekter på lärande vid dövblindhet : möjligheter och begränsningar för personer med Alström syndrom." Licentiate thesis, Örebro universitet, Institutionen för hälsovetenskap och medicin, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-44667.

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Dahlgren, Simon. "The association between cognition and speech-in-noise perception : Investigating the link between speech-in-noise perception and fluid intelligence in people with and without hearing loss." Thesis, Linköpings universitet, Institutionen för datavetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-166708.

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The link between speech-in-noise recognition and cognition has been researched extensively over the years, and the purpose of this thesis was to add to this field. Data from a sample of 394 participants from the n200 database (Rönnberg et al., 2016) was used to calculate the correlation between their performance on a speech-in-noise test and their score on a test measuring fluid intelligence. The speech-in-noise test consisted of matrix sentences with 4-talker babble as noise and fluid intelligence was represented by the score on a Raven’s Progressive Matrices test. Around half of the particip

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Dell\'Aringa, Alfredo Rafael. "Contribuição ao estudo da etiologia das perdas auditivas hereditárias, progressivas e de causas desconhecidas." Universidade de São Paulo, 1999. http://www.teses.usp.br/teses/disponiveis/5/5143/tde-05092014-101309/.

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O autor estudou famílias com surdez hereditária, congênita e de causas desconhecidas, na região da cidade de Marília, Estado de São Paulo (Brasil). Foram analisadas 33 famílias, com 100 pessoas afetadas. A história familiar de cada uma, abrangeu no mínimo três gerações. Todo paciente afetado, e seus familiares, que foram avaliados, submeteram-se a exame otorrinolaringológico, audiológico, laboratorial e radiológico. Heredogramas foram analisados para se avaliar o tipo de transmissão em cada família ( dominante, recessivo, ligado ao cromossomo X, genético desconhecido, não genético e de causa d

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Kii, Márcia Akemi. "Perfil de auto-anticorpos na surdez súbita, surdez rapidamente progressiva e doença de Ménière." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/5/5143/tde-13102014-111008/.

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A surdez neurossensorial imunomediada (SNIM) é uma das formas reversíveis de surdez neurossensorial, justificando a necessidade de identificação de marcadores mais específicos que ajudem na sua abordagem. O Western blot com antígenos de tecidos bovinos detecta um anticorpo contra a proteína de 68kD (hsp-70) em SNIM. Entretanto, anticorpos antihsp- 70 são comumente encontrados em indivíduos sadios. O objetivo do estudo foi determinar a reatividade de soros de pacientes com doenças otológicas freqüentemente relacionadas à etiologia auto-imune contra antígeno celular de linhagem humana (HeLa) atr

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Baganha, Sara Barbosa. "Asymmetric Sensorineural Hearing Loss in Children: progression and involvement of the contralateral ear." Master's thesis, 2021. http://hdl.handle.net/10316/98312.

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Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de Medicina<br>Objective: Sensorineural hearing loss (SNHL) has a profound negative impact on children’s lives. This study aims to examine the progression of asymmetric sensorineural hearing loss in children, according to the baseline hearing thresholds in the worst ear and to the technological level of the hearing aid fitted. Methods: Eighteen children with asymmetric SNHL fitted with a nonlinear hearing aid for more than 2 years were selected for this retrospective study. The participants were interviewed and submitted

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Books on the topic "Progressive hearing loss"

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Heidet, Laurence, Bertrand Knebelmann, and Marie Claire Gubler. Alport syndrome. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0321.

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Alport syndrome is an inherited renal disorder characterized by early haematuria, progressing to proteinuria, sensorineural hearing loss, and progressive renal failure typically in the third or fourth decade but with wide variation. It is responsible for about 1% of end-stage renal failure. Over 80% of cases are X-linked and young men are most affected, but heterozygous carriers of the abnormal gene are also at significantly increased risk of end-stage renal failure in their lifetime. Those affected by the autosomal recessive variant are phenotypically very similar. It is caused by mutations i

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Heidet, Laurence, Bertrand Knebelmann, and Marie Claire Gubler. Alport syndrome. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0322_update_001.

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This chapter describes the clinical features of Alport syndrome. The characteristic features of this familial condition are haematuria with progressive nephropathy and sensorineural hearing loss. Most cases are X-linked so this is typically seen in boys and young men, but female heterozygous (‘carriers’) of X-linked Alport syndrome are also at significant risk of renal disease in their lifetime. The average age of end-stage renal failure is in the third or fourth decade. Those with autosomal recessive disease (approximately 15%) show a similar phenotype. Hearing loss characteristically develop

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Lucas, Joshua, Dawn Fishback, and Steven Giannotta. Skull Base Schwannoma. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0013.

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This chapter presents a case example of a patient with progressive unilateral hearing loss who was ultimately diagnosed with a skull base schwannoma. The workup and differential diagnosis are presented and options for treatment are reviewed based on published evidence. Treatment options include observation, stereotactic radiosurgery, and surgical resection. The objective status of a patient’s hearing as well as the patient’s age influence treatment recommendations and the surgical approach. Intraoperative neuromonitoring provides real-time assessment of facial nerve irritation as well as cochl

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Alport Syndrome. Exon Publications, 2024. http://dx.doi.org/10.36255/alport-syndrome.

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Alport Syndrome is a genetic condition that affects the kidneys, ears, and eyes, causing progressive damage to these organs over time. This article serves as a comprehensive guide to understanding the condition, its causes, and how it is managed. It begins by explaining what Alport Syndrome is and the role of the COL4A3, COL4A4, and COL4A5 genes in causing the disorder. The article explores its prevalence and the different types of inheritance, including X-linked, autosomal recessive, and autosomal dominant patterns, which influence the severity of the condition. The guide details the symptoms

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Tay-Sachs Disease. Exon Publications, 2024. http://dx.doi.org/10.36255/tay-sachs-disease.

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Tay-Sachs Disease is a rare genetic disorder that causes progressive damage to the nervous system, primarily affecting infants and young children. This article begins by explaining the genetic cause of the disease, which involves mutations in the HEXA gene leading to the absence of beta-hexosaminidase A, an enzyme essential for breaking down fatty substances in the brain. It describes the symptoms of the condition, including developmental delays, muscle weakness, vision and hearing loss, and seizures. The diagnostic process is explained, highlighting the role of enzyme testing, genetic analysi

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Book chapters on the topic "Progressive hearing loss"

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Tebbe, Lars, Muayyad R. Al-Ubaidi, and Muna I. Naash. "A Knockin Model with the Mouse Equivalent to the c.2299delG Mutation in Usherin Exhibits Early-Onset Hearing Loss and Progressive Retinal Degeneration." In Advances in Experimental Medicine and Biology. Springer Nature Switzerland, 2025. https://doi.org/10.1007/978-3-031-76550-6_42.

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Naz, Sadaf. "Genetics of Nonsyndromic Recessively Inherited Moderate to Severe and Progressive Deafness in Humans." In Hearing Loss. InTech, 2012. http://dx.doi.org/10.5772/31808.

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"9 Unilateral Slowly Progressive Hearing Loss." In Differential Diagnosis in Otolaryngology-Head and Neck Surgery, edited by Michael G. Stewart and Samuel H. Selesnick. Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/b-0034-81089.

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"Idiopathic Progressive Bilateral Sensorineural Hearing Loss (IPBSNHL)." In Encyclopedia of Otolaryngology, Head and Neck Surgery. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-23499-6_100476.

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Brice, Alejandro. "Noise Induced Hearing Loss: A Case Study from a Speech-Language Pathologist’s Perspective." In Hearing Loss - From Multidisciplinary Teamwork to Public Health. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96332.

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Hearing loss is very common in the United States and the most widespread disability in the U.S. Hearing loss is the third most chronic health condition in the U.S. Noise induced hearing loss (NIHL) results from damaging external noise. This injury leads to temporarily or permanently affecting sensitive inner ear structures (e.g., cochlea, organ of Corti, and hair cells). NIHL can result from a single high-level noise exposure or repeated exposures to excessively loud noises [i.e., typically 85 dBA or greater, (A weighted decibel)]. Damage to the inner ear can also result from aging (i.e., pres

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Toriello, Helga V. "Genetic Hearing Loss Associated with Neurologic and Neuromuscular Disorders." In Hereditary Hearing Loss And Its Syndromes. Oxford University PressNew York, NY, 2004. http://dx.doi.org/10.1093/oso/9780195138498.003.0010.

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Abstract Many progressive neurodegenerative diseases are associated with sensorineural hearing loss, but the classification of these disorders remains controversial. This chapter combines reports of families with similar disorders and different ages of onset, but separates similar families if the pattern of inheritance was different. It is apparent that some neurological manifestations of these diseases tend to cluster. For example, ataxia is frequently associated with spastic paraplegia (“spinocerebellar ataxia”) and with motor and sensory neuropathy. Pigmentary retinopathies (which include r

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Glindzicz, Maria Bitner, Karen E. Heath,, and Angel Campos-Barros. "Genetic Hearing Loss Associated with Renal Disorders." In Hereditary Hearing Loss And Its Syndromes. Oxford University PressNew York, NY, 2004. http://dx.doi.org/10.1093/oso/9780195138498.003.0009.

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Abstract In this chapter, we have attempted to place the conditions considered here into groups such as specific nephritides, nephroses, and renal acidoses. Molecular genetic studies are rapidly clarifying the molecular basis of various syndromes, confirming genetic heterogeneity in some while identifying allelic disorders in others. Alport syndrome (nephritis and sensorineural hearing loss) The syndrome of hereditary progressive glomerulonephritis with intermittent or gross hematuria and sensorineural hearing loss was first described by Alport (I) in 1927. Earlier reports of the same family w

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Mara, Rissatto-Lago. "Hearing Damage Caused by Sickle Cell Disease." In Sickle Cell Disease [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.104705.

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Sickle cell disease (SCD) is a multisystem disease associated with episodes of acute illness and progressive organ damage, leading to impairment of several organs. It is characterized by vaso-occlusive processes resulting from local hypoxia, increased number of sickled erythrocytes, and dissemination of occlusion to adjacent tissues. SCD has a chronic inflammatory mechanism that affects several organs and systems, including the auditory system. Hearing loss resulting from SCD includes conductive hearing loss, sensorineural hearing loss, in the central auditory system, in addition to otoneurolo

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Willott, James F. "Central auditory plasticity in mouse models of progressive sensorineural hearing loss." In Reprogramming the Cerebral Cortex. Oxford University Press, 2006. http://dx.doi.org/10.1093/acprof:oso/9780198528999.003.0009.

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Stevens, Michael. "New Insights into Beethoven’s Deafness." In Pharynx – the Incredible Rendezvous Sites of Gas, Liquid and Solid [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101889.

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There have been many theories proposed to explain the deafness of Ludwig van Beethoven, because his history is complex. Evidence of otosclerosis is lacking, because close gross examination of Beethoven’s middle ear at autopsy did not find any otosclerotic foci. His slowly progressive hearing loss over a period of years differs from the reported cases of autoimmune hearing loss, which is rapidly progressive over a period of months. The absence of mercury in Beethoven’s hair and bone samples leads us to conclude that his deafness was not due to syphilis, because in that era, syphilis was treated

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Conference papers on the topic "Progressive hearing loss"

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Baumgartner, Wolf-Dieter, Faris Brkic, and Alexandra Jappel. "Progressive Sensorineural Hearing Loss in Vibrant Soundbridge Users Requiring Cochlear Implantation." In 94. Jahresversammlung Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1766698.

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Baumgartner, Wolf-Dieter, Faris Brkic, and Alexandra Jappel. "Progressive Sensorineural Hearing Loss in Vibrant Soundbridge Users Requiring Cochlear Implantation." In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767311.

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Momper, Theresa, Robert Mlynski, and Stefanie Rettschlag. "Rare differential diagnosis of a patient with bilateral sensorineural hearing loss and progressive Tinnitus." In 95th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e. V., Bonn. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1784626.

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Babirsoy, Dadash, Tina Brzoska, Friedrich Ihler, and Oliver Dziemba. "Unexpected inadequate speech intelligibility with cochlear implant (CI) in an 81-year-old female patient with progressive hearing loss." In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767326.

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Martinelli, Jose, Jessica Ivanovs, and Marcos Martinelli. "GERIATRIC EVALUATION IN 27 CASES OF MUSICAL HALLUCINATION." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda073.

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Background: Musical hallucination (AM) is a type of complex auditory hallucination described as hearing musical tones, rhythms, harmonies, and melodies without the corresponding external auditory stimulus. This type of hallucination is relatively rare and is seen less often than other types of hallucination. Such hallucinations can be continuous or intermittent and are usually accompanied by a clear and critical awareness on the part of the patient. AM are found mainly in elderly women with progressive hearing loss, usually due to ear diseases or lesions. They also occur in neurological disord

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Soares, Izadora Fonseca Zaiden, João Nicoli Ferreira dos Santos, and Lis Gomes Silva. "Dramatic cognitive improvement with acetylcholinesterase inhibitor in cerebral amyloid angiopathyrelated inflammation." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.578.

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Context: Cerebral amyloid angiopathy (CAA) is characterized by progressive deposition of amyloid-ß fibrils in the walls of small arterioles and capillaries of the leptomeninges and cerebral cortex. A rare subtype of CAA is CAA-related inflammation (CAA-RI), which exhibits marked perivascular or transmural inflammatory infiltration in brain tissue. The major clinical features of CAA-RI are rapidly progressive dementia, behavioral changes, headache, seizures, or stroke-like signs. Conclusive diagnosis requires histopathological confirmation, but validated clinicoradiological criteria for the dia

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Moya, Manoel Vilela, Mariana Laranjeira Pierotti, and Alyosha Fabiana Rodrigues. "Relationship between hearing loss and cognitive memory decline in an elderly population." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.666.

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Background: The major complaints of the elderly are hearing and memory loss, which have a devastating impact on the communication process. Previous studies have shown that hearing loss is associated with the acceleration of this cognitive decline. Objectives: To analyze the relationship between moderate to moderatelysevere hearing loss and memory deficit in elderly individuals. Design and setting: This is an observational, cross-sectional study realized in seniors of Hearing Care Program at the Taubaté University Hospital, Taubaté - SP/ Brazil. Methods: Data was collected using audiometry, ana

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Silva, Bruno Custódio, Tatiane Andressa Gasparetto, Fábio Biguelini Duarte, Paulo Ricardo Gazzola Zen, and Rafael Fabiano Machado Rosa. "Clinical and neurological findings of a patient with type 2 neurofibromatosis." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.069.

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Context: Neurofibromatosis type 2 (NF2) is an autosomal dominant genetic disease that predisposes to tumors development, especially schwannomas involving vestibular nerves. Case report: A 13-year-old girl, a couple’s daughter with no cases of genetic diseases in the family, had photophobia and recurrent left eye paralysis since she was 5 years old. At 11, she had dizziness at rest and on moving. Physical exam showed a lack of balance, weakness in the legs and bilateral papilledema. Cranial computed tomography revealed a bilateral vestibular nerve schwannoma. The increase in tumor volume led to

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Trier, Barbara, Daniel Hirth, Timo Stöver, and Sabine Kramer. "Progression, severity and management of hearing loss in preschool children with congenital CMV infection." In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767529.

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Krech, Lisa, Anja Pähler vor der Holte, Merle Bock, et al. "Health care research project on hearing ability and Dementia in residential care facilities in the greater Hanover area – Progression of hearing loss and Dementia." In 95th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e. V., Bonn. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1785160.

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