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International Journal of Audiology Volume 49, 2010 - Issue 8
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Original Article

Causes of hearing impairment in the Norwegian paediatric cochlear implant program

Geir Siem Department of Otolaryngology, Faculty Division Rikshospitalet, University of Oslo, Norway; Department of Otolaryngology, Oslo University Hospital, Rikshospitalet, Oslo, NorwayCorrespondence[email protected]
,
Toril Fagerheim University Hospital of North Norway, Division of Child and Adolescent Health, Department of Medical Genetics, N-9038 Tromsø, Norway
,
Christoffer Jonsrud University Hospital of North Norway, Division of Child and Adolescent Health, Department of Medical Genetics, N-9038 Tromsø, Norway
,
Claude Laurent Department of Otolaryngology, Oslo University Hospital, Rikshospitalet, Oslo, Norway; Department of Otolaryngology, Faculty Division Rikshospitalet, University of Oslo, Norway
,
Erik Teig Department of Otolaryngology, Oslo University Hospital, Rikshospitalet, Oslo, Norway
,
Sten Harris Department of Otolaryngology, Oslo University Hospital, Rikshospitalet, Oslo, Norway; Department of Otolaryngology, Faculty Division Rikshospitalet, University of Oslo, Norway
,
Trond P. Leren Department of Medical Genetics, Oslo University Hospital, Rikshospitalet, Oslo, Norway
,
Andreas Früh Department of Pediatrics, Oslo University Hospital, Rikshospitalet, Oslo, Norway
&
Ketil Heimdal Department of Medical Genetics, Oslo University Hospital, Rikshospitalet, Oslo, Norway
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Pages 596-605 | Received 29 Jun 2009, Accepted 02 Mar 2010, Published online: 16 Jun 2010

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Niels Krintel Petersen, Anders W. Jørgensen & Therese Ovesen. (2015) Prevalence of various etiologies of hearing loss among cochlear implant recipients: Systematic review and meta-analysis. International Journal of Audiology 54:12, pages 924-932.
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Per-Inge Carlsson, Eva Karltorp, Eva Carlsson-Hansén, Henrik Åhlman, Claes Möller & Ulrika VonDöbeln. (2012) GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort. Acta Oto-Laryngologica 132:12, pages 1301-1305.
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Articles from other publishers (17)

Jekaterina Byckova, Violeta Mikstiene, Silvija Kiveryte, Vaiva Mickeviciene, Margarita Gromova, Gabriele Cernyte, Jurga Mataityte-Dirziene, Daumantas Stumbrys, Algirdas Utkus & Eugenijus Lesinskas. (2020) Etiological profile of hearing loss amongst Lithuanian pediatric cochlear implant users. International Journal of Pediatric Otorhinolaryngology 134, pages 110043.
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Xiaoyu Yu, Hao Wu & Tao Yang. (2019) Molecular basis of hearing loss associated with enlarged vestibular aqueduct. Journal of Bio-X Research 2:3, pages 121-124.
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Violeta Mikstiene, Audrone Jakaitiene, Jekaterina Byckova, Egle Gradauskiene, Egle Preiksaitiene, Birute Burnyte, Birute Tumiene, Ausra Matuleviciene, Laima Ambrozaityte, Ingrida Uktveryte, Ingrida Domarkiene, Tautvydas Rancelis, Loreta Cimbalistiene, Eugenijus Lesinskas, Vaidutis Kucinskas & Algirdas Utkus. (2016) The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. BMC Genetics 17:1.
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Andreas Früh, Geir Siem, Henrik Holmström, Gaute Døhlen & Kristina H. Haugaa. (2016) The Jervell and Lange-Nielsen syndrome; atrial pacing combined with ß-blocker therapy, a favorable approach in young high-risk patients with long QT syndrome?. Heart Rhythm 13:11, pages 2186-2192.
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Nikolay A. Barashkov, Vera G. Pshennikova, Olga L. Posukh, Fedor M. Teryutin, Aisen V. Solovyev, Leonid A. Klarov, Georgii P. Romanov, Nyurgun N. Gotovtsev, Andrey A. Kozhevnikov, Elena V. Kirillina, Oksana G. Sidorova, Lena M. Vasilyevа, Elvira E. Fedotova, Igor V. Morozov, Alexander A. Bondar, Natalya A. Solovyevа, Sardana K. Kononova, Adyum M. Rafailov, Nikolay N. Sazonov, Anatoliy N. Alekseev, Mikhail I. Tomsky, Lilya U. Dzhemileva, Elza K. Khusnutdinova & Sardana A. Fedorova. (2016) Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic). PLOS ONE 11:5, pages e0156300.
Crossref
Xiuhong Pang, Yongchuan Chai, Longxia He, Penghui Chen, Xiaowen Wang, Lei Li, Huan Jia, Hao Wu & Tao Yang. (2015) A 7666-bp genomic deletion is frequent in Chinese Han deaf patients with non-syndromic enlarged vestibular aqueduct but without bi-allelic SLC26A4 mutations. International Journal of Pediatric Otorhinolaryngology 79:12, pages 2248-2252.
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Keita Tsukada, Shin-ya Nishio, Mitsuru Hattori & Shin-ichi Usami. (2015) Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations . Annals of Otology, Rhinology & Laryngology 124:1_suppl, pages 61S-76S.
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Siri Nelson, Ronny Andersen & Sven-Harald Anderssen. (2015) Hørselstap hos barn i Østfold 2000 – 09. Tidsskrift for Den norske legeforening 135:2, pages 132-136.
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Ellen Kvestad, Kari Kveim Lie, Anne Eskild & Bo Engdahl. (2014) Sensorineural hearing loss in children: The association with Apgar score. A registry-based study of 392371 children in Norway. International Journal of Pediatric Otorhinolaryngology 78:11, pages 1940-1944.
Crossref
Lynn M. Pique, Marie-Luise Brennan, Colin J. Davidson, Frederick Schaefer, John Greinwald Jr & Iris Schrijver. (2014) Mutation analysis of the SLC26A4 , FOXI1 and KCNJ10 genes in individuals with congenital hearing loss . PeerJ 2, pages e384.
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Anne-Sofie Skou, Lisbeth Tranebjærg, Tim Jensen & Henrik Hasle. (2014) Mitochondrial 12S Ribosomal RNA A1555G Mutation Associated with Cardiomyopathy and Hearing Loss following High-Dose Chemotherapy and Repeated Aminoglycoside Exposure. The Journal of Pediatrics 164:2, pages 413-415.
Crossref
Dylan K. Chan & Kay W. Chang. (2014) GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 124:2, pages E34-E53.
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ND Rendtorff, I Schrijver, M Lodahl, J Rodriguez-Paris, T Johnsen, EC Hansén, LAA Nickelsen, Z Tümer, T Fagerheim, R Wetke & L Tranebjaerg. (2013) SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations . Clinical Genetics 84:4, pages 388-391.
Crossref
W.F. Burke, T. Lenarz & H. Maier. (2013) Hereditäre SchwerhörigkeitHereditary hearing loss. HNO 61:4, pages 353-363.
Crossref
Víctor Faundes, Rosa Andrea Pardo & Silvia Castillo Taucher. (2012) Genética de la sordera congénita. Medicina Clínica 139:10, pages 446-451.
Crossref
Selena E. Heman-Ackah, J. Thomas RolandJr.Jr., David S. Haynes & Susan B. Waltzman. (2012) Pediatric Cochlear Implantation: Candidacy Evaluation, Medical and Surgical Considerations, and Expanding Criteria. Otolaryngologic Clinics of North America 45:1, pages 41-67.
Crossref
Zenobia Bagli. 2012. Communication Disorders in Multicultural and International Populations. Communication Disorders in Multicultural and International Populations 208 242 .

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