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Journal articles on the topic 'Hearing disorders – Diagnosis'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

BLAETTNER, UWE, MICHAEL SCHERG, and DETLEV VON CRAMON. "DIAGNOSIS OF UNILATERAL TELENCEPHALIC HEARING DISORDERS." Brain 112, no. 1 (1989): 177–95. http://dx.doi.org/10.1093/brain/112.1.177.

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2

Brown, Taylor M., Becky S. Baas, Ruth E. Stoeckel, Lee A. Belf, and Gayla L. Poling. "Assessment of Children With Hearing Loss and Co-Occurring Medical Disorders: Challenging Cases." Perspectives of the ASHA Special Interest Groups 6, no. 2 (April 28, 2021): 375–83. http://dx.doi.org/10.1044/2021_persp-20-00080.

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Purpose Assessing children with hearing loss and co-occurring medical disorders can be challenging. The purpose of this clinical focus article is to highlight multidisciplinary decision making and evaluation considerations when assessing communication skills of children with hearing loss and co-occurring disorders: velopharyngeal insufficiency, childhood apraxia of speech, and autism spectrum disorder. Method Case examples are described to illustrate multidisciplinary decision-making processes for assessing the communication skills of children with hearing loss who have co-occurring velopharyn

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3

Strain, George M. "Hearing disorders in cats: Classification, pathology and diagnosis." Journal of Feline Medicine and Surgery 19, no. 3 (March 2017): 276–87. http://dx.doi.org/10.1177/1098612x17695062.

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Practical relevance: Auditory function is a sense that is central to life for cats - being important in situational awareness of potential predators, pursuit of prey, and for communication with conspecifics, humans and other species. Deafness in cats is most frequently the result of a genetic disorder, strongly associated with white fur and blue eyes, but may also result from acquired causes such as advancing age, ototoxic drugs, infection, environmental noise and physical trauma. Deafness can be sensorineural, where there is loss of cochlear hair cells, or conductive, where sound is muffled o

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Kushalnagar, Poorna, Jennifer Reesman, Tara Holcomb, and Claire Ryan. "Prevalence of Anxiety or Depression Diagnosis in Deaf Adults." Journal of Deaf Studies and Deaf Education 24, no. 4 (August 1, 2019): 378–85. http://dx.doi.org/10.1093/deafed/enz017.

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Abstract The national prevalence of depression and anxiety disorders among deaf adults who use American Sign Language (ASL) remains largely understudied. Data for self-reported depression and anxiety disorder diagnosis (n = 1,704 deaf adults; n = 3,287 hearing adults) as told by their healthcare providers were drawn from HINTS-ASL and HINTS datasets. Chi-square and Poisson regression analysis compared characteristics and predictors for depression or anxiety disorder diagnosis among deaf adults. Rate of diagnosed depression or anxiety disorder was significantly higher (25%) and occurred at earl

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Roberts, Richard A., Gary P. Jacobson, and Kelsey Hatton. "Multiple Co-Occurring Vestibular Disorders Identified Using the Dizziness Symptom Profile." American Journal of Audiology 29, no. 3 (September 3, 2020): 1–9. http://dx.doi.org/10.1044/2020_aja-19-00119.

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Purpose The purpose of the current investigation was to determine the interrelations among vestibular disorders from a data set generated from the patient perspective as compared to previous data generated from the physician's perspective. Method The data for the current investigation originated from a previously published study describing the development of the Dizziness Symptom Profile (DSP; Jacobson et al., 2019 ). The DSP is a 31-item patient self-report tool designed to help primary care physicians in the development of a differential diagnosis using the patient's level of agreement with

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Salata, Tiago Medina, Bruno Niemeyer de Freitas Ribeiro, Bernardo Carvalho Muniz, Lívia de Oliveira Antunes, Heraldo Belmont Rosas, and Edson Marchiori. "Hearing disorders - findings on computed tomography and magnetic resonance imaging: pictorial essay." Radiologia Brasileira 52, no. 1 (February 2019): 54–59. http://dx.doi.org/10.1590/0100-3984.2016.0213.

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Abstract Hearing disorders are usually unilateral and are more common in women. They can be congenital or acquired, and hearing loss is categorized as sensorineural, conductive, or mixed. The onset of hearing loss can be progressive or sudden, and it is a common reason for seeking medical attention. In this context, computed tomography and magnetic resonance imaging have assumed critical roles in the search for an etiological diagnosis and in guiding the therapeutic approach. In this pictorial essay, we illustrate the common causes of hearing loss, discussing the possible differential diagnose

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De Siati, Romolo Daniele, Flora Rosenzweig, Guillaume Gersdorff, Anaïs Gregoire, Philippe Rombaux, and Naïma Deggouj. "Auditory Neuropathy Spectrum Disorders: From Diagnosis to Treatment: Literature Review and Case Reports." Journal of Clinical Medicine 9, no. 4 (April 10, 2020): 1074. http://dx.doi.org/10.3390/jcm9041074.

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Auditory neuropathy spectrum disorder (ANSD) refers to a range of hearing impairments characterized by deteriorated speech perception, despite relatively preserved pure-tone detection thresholds. Affected individuals usually present with abnormal auditory brainstem responses (ABRs), but normal otoacoustic emissions (OAEs). These electrophysiological characteristics have led to the hypothesis that ANSD may be caused by various dysfunctions at the cochlear inner hair cell (IHC) and spiral ganglion neuron (SGN) levels, while the activity of outer hair cells (OHCs) is preserved, resulting in discr

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8

Mahmoudi, Elham, Tanima Basu, Kenneth Langa, Michael McKee, Phillip zazove, and Neil Kamdar. "CAN HEARING AIDS DELAY THE ONSET OF ALZHEIMER’S AND OTHER AGE-RELATED CONDITIONS AMONG ADULTS WITH HEARING LOSS?" Innovation in Aging 3, Supplement_1 (November 2019): S377—S378. http://dx.doi.org/10.1093/geroni/igz038.1385.

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Abstract In this study, we examined the association between hearing aids (HAs) and the onset of Alzheimer’s disease or dementia; depression or anxiety; drug or alcohol disorders; and falls among adults aged 50 and older with hearing loss (HL). We performed a retrospective study of 176,716 adults (50+) with HL diagnoses using a national, insurance claims data (2008-2016). We used Kaplan Meier curves to examine disease-free survival and Cox regression models to examine the risk-adjusted association between HAs and time to diagnosis of 4 age-related/HL-associated conditions within 3 years of HL d

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Martins, Regina Helena Garcia, Henrique Abrantes do Amaral, Elaine Lara Mendes Tavares, Maira Garcia Martins, Tatiana Maria Gonçalves, and Norimar Hernandes Dias. "Voice Disorders: Etiology and Diagnosis." Journal of Voice 30, no. 6 (November 2016): 761.e1–761.e9. http://dx.doi.org/10.1016/j.jvoice.2015.09.017.

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10

Probst, Rudolf. "Hearing and Balance Disorders: Achieving Excellence in Diagnosis and Management." International Journal of Audiology 48, no. 12 (January 2009): 885. http://dx.doi.org/10.3109/14992020802441815.

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11

Kumar, Arun, Meenakshi Jaiswal, and Shelza Shelza. "Survey of classification algorithm used in diagnosis of hearing disorders." International Journal of Advances in Computing and Information Technology 1, no. 2 (April 20, 2012): 195–98. http://dx.doi.org/10.6088/ijacit.12.10025.

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12

Kimberling, William J. "Uncertainties in the molecular diagnosis of recessive hearing loss disorders." Genetics in Medicine 5, no. 4 (July 2003): 259–60. http://dx.doi.org/10.1097/01.gim.0000079363.82988.74.

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Tabibzadeh, Nahid, Dominique Fleury, Delphine Labatut, Frank Bridoux, Arnaud Lionet, Noémie Jourde-Chiche, François Vrtovsnik, Nicole Schlegel, and Philippe Vanhille. "MYH9-related disorders display heterogeneous kidney involvement and outcome." Clinical Kidney Journal 12, no. 4 (December 17, 2018): 494–502. http://dx.doi.org/10.1093/ckj/sfy117.

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AbstractBackgroundMYH9-related diseases (MYH9-RD) are autosomal dominant disorders caused by mutations of the MYH9 gene encoding the non-muscle myosin heavy chain IIA. They are characterized by congenital thrombocytopenia, giant platelets and leucocyte inclusions. Hearing impairment, pre-senile cataract and nephropathy can also occur. We aimed to evaluate renal involvement and outcome in MYH9-RD patients followed-up by nephrologists.MethodsWe conducted a retrospective multicentre observational study of 13 patients among 9 families with MYH9 mutation diagnosed by genetic testing and immunofluor

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Khavidaki, Gholam-Ali Dashti, and Reza Gharibi. "Evaluation of the effectiveness of newborn hearing screening program in Zahedan: A cross-sectional study." Pakistan Journal of Medical and Health Sciences 15, no. 6 (June 30, 2021): 2067–71. http://dx.doi.org/10.53350/pjmhs211562067.

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Introduction: Hearing loss is one of the most common congenital disorders. The prevalence of this disorder in different communities has been reported between 3.5 to 9 percent, which can have adverse effects on language learning, communication, and education of children. Also, early diagnosis of this disorder in newborns is not possible without the use of hearing screening. Therefore, the aim of this study was to evaluate the effectiveness of newborn hearing screening programs in Zahedan. Method: In this cross-sectional observational study, all babies born in the maternity hospitals of Zahedan

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Karimova, N. A., Sh D. Islomov, and Sh E. Amonov. "Features of objective audiometry tests and their diagnostic value in the research of hearing in children." OTORHINOLARYNGOLOGY, no. 4-5(2) 2019 (March 12, 2020): 53–57. http://dx.doi.org/10.37219/2528-8253-2019-4-53.

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The article highlights the features of the conduct and interpretation of data on audiological tests at the children in order to identify the degree, type and level of damage of the auditory disorders. According to a survey of 121 children with a diagnosis of sensorineural hearing loss, it was confirmed that using a complex algorithm of audiological tests such as OAE, DPOAE, BERA and ASSR in hearing diagnosis of the children allows to obtain more accurate and detailed information and avoid possible errors in determining various forms of hearing disorders.

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Svatko, L. G., and I. L. Sobol. "The value of ultrasound in the diagnosis of auditory disorders in cervical osteochondrosis." Kazan medical journal 67, no. 6 (November 15, 1986): 459–60. http://dx.doi.org/10.17816/kazmj70931.

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We performed a comprehensive audiometric examination of 105 patients with hearing impairment due to cervical osteochondrosis. The correlation between the lesion of the auditory analyzer and cervical osteochondrosis was considered absolutely proven if hearing improvement was observed as a result of manual therapy of the cervical spine.

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Veldman, Jan E. "Cochlear and Retrocochlear Immune-Mediated Inner Ear Disorders." Annals of Otology, Rhinology & Laryngology 95, no. 5 (September 1986): 535–40. http://dx.doi.org/10.1177/000348948609500518.

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Three different forms of immune-mediated sensorineural hearing loss are described. The pathogeneses of these three cases with severe audiovestibular deficits are completely different. To make an appropriate diagnosis remains a dilemma. Autoimmunity plays a certain role, but is not always present. Vascular and neural tissue can become involved. Immune-mediated forms of sensorineural hearing loss can be of cochlear or retrocochlear origin.

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18

Abe, Masako. "Diagnosis and Treatment of Articulation Disorders." Japan Journal of Logopedics and Phoniatrics 43, no. 3 (2002): 316–24. http://dx.doi.org/10.5112/jjlp.43.316.

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19

Tufatulin, G. Sh, I. V. Koroleva, S. A. Artyushkin, and Yu K. Yanov. "Complex disorders in children with sensorineural hearing loss — influence on the diagnosis of hearing pathology and hearing aid." Vestnik otorinolaringologii 85, no. 4 (2020): 30. http://dx.doi.org/10.17116/otorino20208504130.

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20

Kleijwegt, Maarten, Floris Bettink, Martijn Malessy, Hein Putter, and Andel van der Mey. "Clinical Predictors Leading to Change of Initial Conservative Treatment of 836 Vestibular Schwannomas." Journal of Neurological Surgery Part B: Skull Base 81, no. 01 (February 4, 2019): 015–21. http://dx.doi.org/10.1055/s-0039-1678708.

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Objective This study was aimed to determine the role of clinical presentation and tumor characteristics in vestibular schwannoma (VS) at diagnosis, initially treated with conservative management. Design The study was designed as a retrospective chart review. Setting The study was prepared at national tertiary referral center for VS patients. Participants A total of 836 VS patients, initially treated conservatively, were included. Main Outcome Measures Patient characteristics: age at diagnosis, gender, frequency, and duration of, hearing loss, tinnitus, balance disorder (unsteadiness, dizziness

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21

Lazareva, L. A., S. A. Azamatova, A. G. Kekeliya, E. V. Zhugan, L. V. Tsyplenkov, B. R. Muzaeva, and I. S. Elizbaryan. "Hearing impairment screening in adults with chronic general somatic pathology in the republic of Adygeya." Kuban Scientific Medical Bulletin 27, no. 5 (October 14, 2020): 46–59. http://dx.doi.org/10.25207/1608-6228-2020-27-5-46-59.

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Background. The steadily growing number of hearing-impaired patients incited epidemiological research into the etiopathogenesis of sensorineural hearing loss.Objectives. To conduct a screening survey of hearing-impaired adults to identify early sensorineural hearing loss in patients with chronic general somatic pathology in the Republic of Adygea.Мethods. We used a screening method for auditory function disorder diagnosis based on surveying patients with no primary hearing complaints. A total of 6,346 patients with variant chronic general somatic pathology were surveyed anonymously. Statistica

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Matthews-Brzozowska, Teresa, Dorota Hojan-Jezierska, Wawrzyniec Loba, Marta Worona, and Artur Matthews-Brzozowski. "Cleidocranial dysplasia-dental disorder treatment and audiology diagnosis." Open Medicine 13, no. 1 (March 1, 2018): 1–8. http://dx.doi.org/10.1515/med-2018-0001.

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AbstractA review of numerous case reports was made, in order to demonstrate the possibilities for treatment of dental disorders in patients with Cleidocranial dysplasia (CCD). In this paper, our own report, including a diagnosis of the effect on the auditory system, is presented. In addition to the triad of CCD symptoms that include hypoplastic or aplastic clavicles, impacted and supernumerary teeth, delayed closure of fontanelles and cranial sutures, impairment of the hearing system resulting in conductive hearing loss also occurs. Our own report is based on the case of a 12-year-old CCD pati

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23

Ralli, Massimo, Maria Romani, Alessio Zodda, Francesca Yoshie Russo, Giancarlo Altissimi, Maria Patrizia Orlando, Maria Gloria Cammeresi, Roberta Penge, and Rosaria Turchetta. "Hyperacusis in Children with Attention Deficit Hyperactivity Disorder: A Preliminary Study." International Journal of Environmental Research and Public Health 17, no. 9 (April 27, 2020): 3045. http://dx.doi.org/10.3390/ijerph17093045.

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The association between hyperacusis and developmental disorders such as autism spectrum disorders has been extensively reported in the literature; however, the specific prevalence of hyperacusis in attention deficit hyperactivity disorder (ADHD) has never been investigated. In this preliminary study, we evaluated the presence of hyperacusis in a small sample of children affected by ADHD compared to a control group of healthy children. Thirty normal hearing children with a diagnosis of ADHD and 30 children matched for sex and age were enrolled in the study. All children underwent audiological a

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Mathews, J., S. Rao, and B. N. Kumar. "Autoimmune sensorineural hearing loss: is it still a clinical diagnosis?" Journal of Laryngology & Otology 117, no. 3 (March 2003): 212–14. http://dx.doi.org/10.1258/002221503321192548.

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Inner ear involvement with sensorineural hearing loss (SNHL) has been reported in many autoimmune disorders including ulcerative colitis. The pathogenetic mechanism of hearing loss in ulcerative colitis is thought to be immune mediated. Diagnostic tests are being developed to identify inner ear autoantibodies, that may be the cause of such hearing loss. The only test that is currently available for clinical use is the Otoblot test. This, however, tests only for antibodies against bovine heat shock protein 70 which is only one of the many cross-reacting proteins against the inner ear in suspect

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Tsirulnikov, E. M., I. A. Vartanyan, G. V. Gersuni, A. S. Rosenblyum, V. I. Pudov, and L. R. Gavrilov. "Use of amplitude-modulated focused ultrasound for diagnosis of hearing disorders." Ultrasound in Medicine & Biology 14, no. 4 (January 1988): 277–85. http://dx.doi.org/10.1016/0301-5629(88)90093-2.

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Greening, Neville K. "Foundations in Autism Spectrum Disorders and Related Neurodevelopmental Disorders: Possible Causes, Characteristics, Diagnosis, and Treatment." Advances in Social Sciences Research Journal 7, no. 7 (July 25, 2020): 293–318. http://dx.doi.org/10.14738/assrj.77.8609.

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Autism Spectrum Disorders (ASD) is a long life formative dysfunction characterized by symptomatic criteria that begins early in infants and continues throughout life. ASD is a condition that influences a child's sensory system that includes touch, smell, taste, hearing, and visual abilities. Typical forms of ASD in the pre-2013 DSM-5 manual also include Asperger's Syndrome; and Pervasive Developmental Disorder. The characteristics of these disorders are similar but may differ significantly. Children with ASD show difficulties or delays with social communication and necessary daily activities.

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McLaughlin, Susan A., John C. Thorne, Tracy Jirikowic, Tiffany Waddington, Adrian K. C. Lee, and Susan J. Astley Hemingway. "Listening Difficulties in Children With Fetal Alcohol Spectrum Disorders: More Than a Problem of Audibility." Journal of Speech, Language, and Hearing Research 62, no. 5 (May 21, 2019): 1532–48. http://dx.doi.org/10.1044/2018_jslhr-h-18-0359.

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Purpose Data from standardized caregiver questionnaires indicate that children with fetal alcohol spectrum disorders (FASDs) frequently exhibit atypical auditory behaviors, including reduced responsivity to spoken stimuli. Another body of evidence suggests that prenatal alcohol exposure may result in auditory dysfunction involving loss of audibility (i.e., hearing loss) and/or impaired processing of clearly audible, “suprathreshold” sounds necessary for sound-in-noise listening. Yet, the nexus between atypical auditory behavior and underlying auditory dysfunction in children with FASDs remains

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Stone, Jennifer, Edwin Rubel, Robert E. Hillman, Matthew Cutter, Shannon C. Mauszycki, Robert V. Shannon, Julius Fridriksson, et al. "The Future Present." ASHA Leader 18, no. 1 (January 2013): 36–47. http://dx.doi.org/10.1044/leader.ftr1.18012013.36.

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Rechitskaya, E. G., and N. A. Belaya. "Differential diagnosis as one of the conditions for proper rehabilitation of cochlear implanted children." Science and School, no. 1, 2020 (2020): 172–76. http://dx.doi.org/10.31862/1819-463x-2020-1-172-176.

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The article considers the importance of differential diagnostics for the qualification of impaired development of children with hearing disabilities, in particular cochlear implanted children. The role of taking into account the structure of the defect in case of impaired hearing and the results of differential diagnosis of speech failure in children with hearing disorders is highlighted in order to determine the priority role of surdopedagogic work in rehabilitation of children after cochlear implantation. Opinions are expressed about the integrated participation of specialists in various fie

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Vermiglio, Andrew J. "On the Clinical Entity in Audiology: (Central) Auditory Processing and Speech Recognition in Noise Disorders." Journal of the American Academy of Audiology 25, no. 09 (October 2014): 904–17. http://dx.doi.org/10.3766/jaaa.25.9.11.

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Background: The area of (central) auditory processing disorder [(C)APD] is highly controversial. This controversy is fueled in part by multiple ambiguous descriptions of this condition. The American Speech-Language and Hearing Association and the American Academy of Audiology state that (C)APD is a clinical entity, but other sources say that this is questionable. The clinical entity is a concept used to define the nature of a disorder in order to facilitate diagnosis and intervention. Nosography is the study of the systematic description of diseases and disorders. The work in the field of noso

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Mullin, Nova, Olivia Mcphee, Cathie Morrow, and Ahmed Youssef. "Assessment, diagnosis and management of the dizzy patient." British Journal of Hospital Medicine 81, no. 12 (December 2, 2020): 1–7. http://dx.doi.org/10.12968/hmed.2020.0469.

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Dizziness and balance disorders are very common problems. Having a structured approach, including adequate history taking and clinical examination, in a multidisciplinary environment allows for effective management of patients with these complex symptoms. Hearing assessment is an integral part of the assessment of patients with dizziness, along with the occasional need for further testing. Identifying red flags, along with the ability to involve different medical specialties, are prerequisites for safe management and a successful outcome. While surgical intervention has a small role in the man

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Kuk, Francis, Amy Jackson, Denise Keenan, and Chi-chuen Lau. "Personal Amplification for School-Age Children with Auditory Processing Disorders." Journal of the American Academy of Audiology 19, no. 06 (June 2008): 465–80. http://dx.doi.org/10.3766/jaaa.19.6.3.

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Background: Children with auditory processing disorders (APD) are described to have a signal-to-noise ratio (SNR) difficulty. Frequency-modulated (FM) systems have been reported to improve this situation. Yet the use of personal amplification that may be more portable has not been attempted. Purpose: To determine whether personal amplification would result in improvement in speech-in-noise performances (attentiveness and speech recognition) and daily functioning in children with diagnosed APD. In addition, the desired hearing aid features (such as required gain, directional microphone and nois

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Cohen, Jonathan. "On the differential diagnosis of reading, attentional and depressive disorders." Annals of Dyslexia 44, no. 1 (January 1994): 165–84. http://dx.doi.org/10.1007/bf02648160.

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Bantwal, Anuradha R. "(Central) Auditory Processing Disorders: Issues and Challenges in India." Perspectives on Global Issues in Communication Sciences and Related Disorders 1, no. 2 (September 2011): 55–63. http://dx.doi.org/10.1044/gics1.2.55.

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Abstract Individuals with (Central) Auditory Processing Disorder, or (C)APD, form a heterogeneous group. The American Speech-Language-Hearing Association has listed the auditory processes that could be assessed to enable diagnosis of (C)APD. In India, detailed audiological assessment and intervention for auditory processing problems is being conducted in relatively few centers. The linguistic diversity of India presents with a unique challenge in providing clinical services and having complete test batteries in all spoken languages. In recent years, (C)APD has generated significant interest am

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Iliadou, Vasiliki Vivian, Gail D. Chermak, and Doris-Eva Bamiou. "Differential Diagnosis of Speech Sound Disorder (Phonological Disorder): Audiological Assessment beyond the Pure-tone Audiogram." Journal of the American Academy of Audiology 26, no. 04 (April 2015): 423–35. http://dx.doi.org/10.3766/jaaa.26.4.9.

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Background: According to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, diagnosis of speech sound disorder (SSD) requires a determination that it is not the result of other congenital or acquired conditions, including hearing loss or neurological conditions that may present with similar symptomatology. Purpose: To examine peripheral and central auditory function for the purpose of determining whether a peripheral or central auditory disorder was an underlying factor or contributed to the child’s SSD. Research Design: Central auditory processing disorder clinic pediat

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Wassef, David W., Nehal Dhaduk, Savannah C. Roy, Gregory L. Barinsky, and Evelyne Kalyoussef. "Helping Children with Special Needs: Who Receives Tympanostomy Tubes?" Annals of Otology, Rhinology & Laryngology 130, no. 8 (January 16, 2021): 954–60. http://dx.doi.org/10.1177/0003489420987425.

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Objectives: Tympanostomy tubes can prevent sequelae of otitis media that adversely affect long term hearing and language development in children. These negative outcomes compound the existing difficulties faced by children who are already diagnosed with developmental disorders. This study aims to characterize this subset of children with developmental disorders undergoing myringotomy and tympanostomy tube insertion. Methods: A retrospective review using the Kids’ Inpatient Database (KID) was conducted, with codes from International Classification of Diseases, Ninth Revision used to query data

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V.B, Piatto, Secches L.V., Arroyo M.A.S., Lopes A.C.P., and Maniglia J.V. "Nonsyndromic Deafness - Molecular Update." Open Biology Journal 2, no. 1 (August 27, 2009): 80–90. http://dx.doi.org/10.2174/1874196700902010080.

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In most cases, hearing loss is a disorder caused by both genetic and environmental factors. The molecular description of deafness has experienced remarkable progress in the last decade, and it is emerging from the use of contemporary methods of cell and molecular biology. Currently, through the application of clinical and molecular genetics it is possible to identify genes associated with inherited, nonsyndromic deafness, and balance dysfunctions of the human cochlea. This brief review provides insights into nonsyndromic hearing loss, since the identification of the molecular basis for the inn

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Umrigar, Ayesha, Amanda Musso, Danielle Mercer, Annette Hurley, Cassondra Glausier, Mona Bakeer, Michael Marble, Chindo Hicks, and Fern Tsien. "Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss." SAGE Open Medical Case Reports 5 (January 1, 2017): 2050313X1774590. http://dx.doi.org/10.1177/2050313x17745904.

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Advances in sequencing technologies and increased understanding of the contribution of genetics to congenital sensorineural hearing loss have led to vastly improved outcomes for patients and their families. Next-generation sequencing and diagnostic panels have become increasingly reliable and less expensive for clinical use. Despite these developments, the diagnosis of genetic sensorineural hearing loss still presents challenges for healthcare providers. Inherited sensorineural hearing loss has high levels of genetic heterogeneity and variable expressivity. Additionally, syndromic hearing loss

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Diao, M., F. Tian, and J. Sun. "Sudden sensorineural hearing loss as the first manifestation of chronic myeloid leukaemia: case report." Journal of Laryngology & Otology 128, no. 11 (November 2014): 1015–17. http://dx.doi.org/10.1017/s0022215114002102.

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AbstractBackground:Sudden sensorineural hearing loss rarely occurs in patients with chronic myeloid leukaemia.Case report:We present a case report of a patient who presented with sudden sensorineural hearing loss as the first manifestation of chronic myeloid leukaemia, and review the mechanisms responsible for sudden sensorineural hearing loss in leukaemic patients.Results:A 31-year-old female presented to our clinic with unilateral sudden sensorineural hearing loss and tinnitus. Pure tone audiometry revealed profound sensorineural hearing loss in the left ear at all frequencies. During an inv

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Jurczak, Piotr, Katarzyna Ita Bieńkowska, Joanna Wrońska, Alicja Miller, Paweł Rygiel, Honorata Urbanek, Łukasz Rolniak, et al. "Summary of the scientific/educational conference titled "State-of-the-art methods of diagnosis, treatment, and rehabilitation of patients with hearing disorders" held on the occasion of the 50th anniversary of the Otorhinolaryngology Department in Krosno." Polski Przegląd Otorynolaryngologiczny 8, no. 2 (May 30, 2019): 68–71. http://dx.doi.org/10.5604/01.3001.0013.2052.

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On January 11, 2019, more than 200 specialists, including physicians, speech therapists, and physiotherapists, gathered in Krosno for a discussion on current problems in diagnosis, treatment, and rehabilitation of patients with hearing disorders. The Conference was held to mark the 50th Anniversary of the establishment of the Otorhinolaryngology Department at the John Paul II Subcarpathian Regional Hospital in Krosno. However, it was the future rather than history that became the main focus of the discussion. The need to continue the tradition of interdisciplinary approach to audiological trea

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Armakov, Sergey. "Causes and Types of Sensorineural Hearing Loss. Clinical Manifestations and Basic Principles of Treatment." Spravočnik vrača obŝej praktiki (Journal of Family Medicine), no. 9 (August 27, 2020): 9–16. http://dx.doi.org/10.33920/med-10-2009-01.

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Sensorineural hearing loss is a disorder associated with the damage to the inner ear structures: the cochlea (cortical organ), dysfunctioning of the vestibule-cochlear nerve or the central part of the auditory analyser (brain stem and cortical representation of the cortical temporal lobe). In recent years, there has been a steady increase in ensorineural hearing loss patients; they account for ca. 70% among the total patients with impaired hearing. The disease has numerous causes and a complex pathogenesis. Among the main factors contributing to hearing loss are genetic predisposition, perinat

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Lee, Tung-Lin, Pei-Hsuan Lin, Pei-Lung Chen, Jin-Bon Hong, and Chen-Chi Wu. "Hereditary Hearing Impairment with Cutaneous Abnormalities." Genes 12, no. 1 (December 30, 2020): 43. http://dx.doi.org/10.3390/genes12010043.

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Syndromic hereditary hearing impairment (HHI) is a clinically and etiologically diverse condition that has a profound influence on affected individuals and their families. As cutaneous findings are more apparent than hearing-related symptoms to clinicians and, more importantly, to caregivers of affected infants and young individuals, establishing a correlation map of skin manifestations and their underlying genetic causes is key to early identification and diagnosis of syndromic HHI. In this article, we performed a comprehensive PubMed database search on syndromic HHI with cutaneous abnormalit

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PİŞTAV AKMEŞE, Pelin, Nilay KAYHAN, Gülce KİRAZLI, and Tayfun KİRAZLI. "İşitme kayıplı çocukların eğitimine ilişkin odyoloji ve konuşma bozuklukları uzmanları görüşleri." Turkish Journal of Audiology And Hearing Research 4, no. 2 (August 2021): 37–44. http://dx.doi.org/10.34034/tjahr.23280.

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Opinions of audiology and speech disorders specialists on education of children with hearing loss Aim: It was aimed to examine the opinions of audiology and speech disorders specialists (ASDS) working with children with hearing loss between the ages of 0-3 in special education and rehabilitation centers on supporting the language development of children and cooperation with the family in communication and speech development. Materials and Methods: Semi-structured interview technique was used in the study conducted with qualitative research method in descriptive design. The data were collected

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Vielsmeier, Veronika, Tobias Kleinjung, Jürgen Strutz, Ralf Bürgers, Peter Michael Kreuzer, and Berthold Langguth. "Tinnitus with Temporomandibular Joint Disorders." Otolaryngology–Head and Neck Surgery 145, no. 5 (June 25, 2011): 748–52. http://dx.doi.org/10.1177/0194599811413376.

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Objective. Tinnitus is frequently associated with temporomandibular joint (TMJ) dysfunction. However, the nature of the relationship is not fully understood. Here the authors compared 30 patients with a confirmed diagnosis of temporomandibular joint dysfunction and tinnitus to a group of 61 patients with tinnitus but without any subjective complaints of TMJ dysfunction with respect to clinical and demographic characteristics. Study Design. Case-control study. Setting. Tertiary referral center. Subjects. Tinnitus patients with and without TMJ dysfunction presenting at the Department of Prosthet

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Gáborján, Anita, Judit Götze, Marianna Küstel, Nóra Kecskeméti, Ildikó Baranyi, Fatime Csontos, and László Tamás. "Az újszülöttkori objektív hallásszűrés utánvizsgálatának eredményei." Orvosi Hetilap 160, no. 47 (November 2019): 1850–55. http://dx.doi.org/10.1556/650.2019.31604.

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Abstract: Sufficient hearing is the cornerstone of the development of children’s complex sensory perception, sound recognition, speech development and optimal communication skills. Hearing screening of newborns is necessary to detect congenital hearing disorders. Compulsory objective hearing screening in Hungary is a significant improvement in early diagnosis. The Audiological Department of Otorhinolaryngology, Head and Neck Surgery Clinic at Semmelweis University serves as a verification center for children identified via the compulsory objective newborn hearing screening and necessitates mor

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Jin, Jingyu Linna, Carolyn Baylor, and Kathryn Yorkston. "Predicting Communicative Participation in Adults Across Communication Disorders." American Journal of Speech-Language Pathology 30, no. 3S (June 18, 2021): 1301–13. http://dx.doi.org/10.1044/2020_ajslp-20-00100.

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Purpose The purpose of this study was to explore the extent to which communicative participation differs across diagnoses and if there are common predictor variables for communicative participation across diagnoses. Method Survey data on self-report variables including communicative participation were collected from 141 community-dwelling adults with communication disorders due to Parkinson's disease, cerebrovascular accident, spasmodic dysphonia, or vocal fold immobility (VFI). Analysis of covariance was used to determine communicative participation differences between diagnoses, with age, se

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Adhikari, Tika Ram, and Thinley Dorji. "Recurrent ear bleed with profound bilateral sensorineural hearing loss: A case of Munchausen syndrome." SAGE Open Medical Case Reports 9 (January 2021): 2050313X2110008. http://dx.doi.org/10.1177/2050313x211000869.

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Factitious disorders and Munchausen syndromes present with history and physical symptoms to all specialties, and they are often extensively evaluated. Diagnosis of Munchausen syndrome is a challenge and patients often do not receive the correct diagnosis and appropriate care especially in settings where access to mental health professionals is difficult. We present a case of recurrent bleed from the right ear, bilateral profound hearing loss and jerky movement of limbs that was extensively evaluated and followed up for 4 years until a diagnosis of Munchausen syndrome was reached. This case rep

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Palomo-Carrión, Rocío, Rita Pilar Romero-Galisteo, Helena Romay-Barrero, Inés Martínez-Galán, Cristina Lirio-Romero, and Elena Pinero-Pinto. "How Does the Cause of Infantile Hemiparesis Influence Other Conditioning Factors? A Preliminary Study in a Spanish Population." Children 8, no. 5 (April 22, 2021): 323. http://dx.doi.org/10.3390/children8050323.

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Infantile hemiparesis may be associated with significant morbidity and may have a profound impact on a child’s physical and social development. Infantile hemiparesis is associated with motor dysfunction as well as additional neurologic impairments, including sensory loss, mental retardation, epilepsy, and vision, hearing, or speech impairments. The objective of this study was to analyze the association between the cause of infantile hemiparesis and birth (gestational age), age of diagnosis, and associated disorders present in children with infantile hemiparesis aged 0 to 3 years. An observatio

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Ralli, Massimo, Giuseppe Nola, Luca Sparvoli, and Giovanni Ralli. "Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops." Case Reports in Otolaryngology 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/6195317.

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Enlarged vestibular aqueduct (EVA) syndrome is a common congenital inner ear malformation characterized by a vestibular aqueduct with a diameter larger than 1.5 mm, mixed or sensorineural hearing loss that ranges from mild to profound, and vestibular disorders that may be present with a range from mild imbalance to episodic objective vertigo. In our study, we present the case of a patient with unilateral enlarged vestibular aqueduct and bilateral endolymphatic hydrops (EH). EH was confirmed through anamnestic history and audiological exams; EVA was diagnosed using high-resolution CT scans and

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Ha, Seunghee, and Dong Gi Seo. "Articulatory Consistency for Differential Diagnosis of Speech Sound Disorders." Communication Sciences & Disorders 24, no. 4 (December 31, 2019): 1015–25. http://dx.doi.org/10.12963/csd.19667.

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