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59 results

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Page 1
Impact of Genetic Testing on Hearing Interventions.
Brodie KD, Liao EN, Florentine MM, Chan DK. Brodie KD, et al. Laryngoscope. 2023 Aug;133(8):1982-1986. doi: 10.1002/lary.30409. Epub 2022 Sep 27. Laryngoscope. 2023. PMID: 36165585
OBJECTIVE: Clinical guidelines recommend genetic testing when evaluating congenital and late-onset sensorineural hearing loss (SNHL). Genetic diagnoses can provide parents additional information regarding anticipated hearing loss progression, comorbid …
OBJECTIVE: Clinical guidelines recommend genetic testing when evaluating congenital and late-onset sensorineural hearing loss …
Does universal newborn hearing screening impact the timing of deafness treatment?
Faistauer M, Silva AL, Dominguez DOR, Bohn R, Félix TM, Costa SSD, Rosito LPS. Faistauer M, et al. J Pediatr (Rio J). 2022 Mar-Apr;98(2):147-154. doi: 10.1016/j.jped.2021.04.008. Epub 2021 Jun 21. J Pediatr (Rio J). 2022. PMID: 34166624 Free PMC article.
METHODS: A retrospective cohort study with children up to 12 years old with bilateral hearing loss were divided into two groups: patients who underwent UNHS and the ones who didn't. ...However, children who passed the screening but were later diagnosed with …
METHODS: A retrospective cohort study with children up to 12 years old with bilateral hearing loss were divided into tw …
Effectiveness of universal newborn hearing screening: A systematic review and meta-analysis.
Edmond K, Chadha S, Hunnicutt C, Strobel N, Manchaiah V, Yoshinga-Itano C; Universal Newborn Hearing Screening (UNHS) review group. Edmond K, et al. J Glob Health. 2022 Oct 19;12:12006. doi: 10.7189/jogh.12.12006. J Glob Health. 2022. PMID: 36259421 Free PMC article.
BACKGROUND: Permanent bilateral hearing loss (PBHL) is a serious condition in newborns, with a prevalence of at least one per 1000 live births. However, there has been no recent systematic review and meta-analysis of the effectiveness of universal newborn …
BACKGROUND: Permanent bilateral hearing loss (PBHL) is a serious condition in newborns, with a prevalence of at least o …
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management.
Tawalbeh M, Aburizeg D, Abu Alragheb BO, Alaqrabawi WS, Dardas Z, Srour L, Altarayra BH, Zayed AA, El Omari Z, Azab B. Tawalbeh M, et al. Genes (Basel). 2022 Nov 23;13(12):2192. doi: 10.3390/genes13122192. Genes (Basel). 2022. PMID: 36553459 Free PMC article.
SLC26A4 is one of the most common genes causing autosomal recessive non-syndromic sensorineural hearing loss (SNHL). It has been reported to cause Pendred Syndrome (PDS) and DFNB4 which is deafness with enlarged vestibular aqueduct (EVA). ...Three unrelated Jordania …
SLC26A4 is one of the most common genes causing autosomal recessive non-syndromic sensorineural hearing loss (SNHL). It has be …
Newborn Hearing Screening: Early Ear Examination Improves the Pass Rate.
Schwarz Y, Mauthner R, Kraus O, Gluk O, Globus O, Kariv L, Tamir SO. Schwarz Y, et al. J Int Adv Otol. 2023 Oct;19(5):402-406. doi: 10.5152/iao.2023.22987. J Int Adv Otol. 2023. PMID: 37789627 Free PMC article.
BACKGROUND: Temporary conductive hearing loss due to vernix accumulation in the external ear canal may lead to a false-positive result in newborn hearing screening tests. ...Twelve of the remaining 14 ears passed at 10-day rescreening. The remaining 2 ears pr …
BACKGROUND: Temporary conductive hearing loss due to vernix accumulation in the external ear canal may lead to a false-positiv …
Universal newborn hearing screening in the Italian Region of Sicily in 2018.
Ferlito S, Maniaci A, Cocuzza S, La Mantia I, Di Mauro P, Poli G, Maiolino L, Coco S, Merlino F, Maltese M, Ragliani M, Russo M, Gulino A, Azieli C, Martines F, Galletti F, Bubbico L. Ferlito S, et al. Acta Otorhinolaryngol Ital. 2021 Aug;41(4):356-363. doi: 10.14639/0392-100X-N1162. Acta Otorhinolaryngol Ital. 2021. PMID: 34533539 Free PMC article.
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss, number of infants "referred" to transiently evoked otoacoustic emissions (TEOAE), number of infants with pathologic auditory brainstem res …
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss …
Universal neonatal hearing screening and delayed hearing loss or late-developmental hearing loss.
Núñez Batalla FJ, Fernández-Cedrón Bermejo C, Guntín García M, Sandoval Menéndez I, Fresno Díaz E, Gómez Martínez JR, Llorente Pendás JL. Núñez Batalla FJ, et al. Acta Otorrinolaringol Esp (Engl Ed). 2023 Sep-Oct;74(5):283-289. doi: 10.1016/j.otoeng.2022.10.007. Epub 2023 May 4. Acta Otorrinolaringol Esp (Engl Ed). 2023. PMID: 37149133
RESULTS: 52 cases met the inclusion criteria. The detection rate of congenital hearing loss in the neonatal screening programme in the same study period was 1.5 children per thousand newborns per year, adding postnatal hearing loss results in a rate of …
RESULTS: 52 cases met the inclusion criteria. The detection rate of congenital hearing loss in the neonatal screening programm …
Audiologists' perspectives on management of mild bilateral hearing loss in infants and young children.
Ching TYC, Saetre-Turner M, Marnane V, Scarinci N, Choik C, Tulloch K, Sung V. Ching TYC, et al. Int J Audiol. 2022 Sep;61(9):752-760. doi: 10.1080/14992027.2021.1961170. Epub 2021 Aug 9. Int J Audiol. 2022. PMID: 34370600
OBJECTIVE: Universal newborn hearing screening programs have led to early identification of infants with congenital mild bilateral hearing loss (MBHL). The current lack of evidence-based protocols to guide audiological management of infants with MBHL h …
OBJECTIVE: Universal newborn hearing screening programs have led to early identification of infants with congenital mild bilateral …
Genetic Testing for Congenital Bilateral Hearing Loss in the Context of Targeted Cytomegalovirus Screening.
Peterson J, Nishimura C, Smith RJH. Peterson J, et al. Laryngoscope. 2020 Nov;130(11):2714-2718. doi: 10.1002/lary.28536. Epub 2020 Jan 27. Laryngoscope. 2020. PMID: 31985074 Free PMC article.
OBJECTIVES/HYPOTHESIS: To determine the prevalence of children with genetic hearing loss who are cytomegalovirus (CMV) positive at birth and the relative proportion of genetic and CMV etiology among children with congenital bilateral hearing loss …
OBJECTIVES/HYPOTHESIS: To determine the prevalence of children with genetic hearing loss who are cytomegalovirus (CMV) positiv …
Audibility-Based Hearing Aid Fitting Criteria for Children With Mild Bilateral Hearing Loss.
McCreery RW, Walker EA, Stiles DJ, Spratford M, Oleson JJ, Lewis DE. McCreery RW, et al. Lang Speech Hear Serv Sch. 2020 Jan 8;51(1):55-67. doi: 10.1044/2019_LSHSS-OCHL-19-0021. Epub 2020 Jan 8. Lang Speech Hear Serv Sch. 2020. PMID: 31913801 Free PMC article.
Purpose Because of uncertainty about the level of hearing where hearing aids should be provided to children, the goal of the current study was to develop audibility-based hearing aid candidacy criteria based on the relationship between unaided hearing …
Purpose Because of uncertainty about the level of hearing where hearing aids should be provided to children, the goal of the c …
59 results