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Original Article

Auditory Function in Hereditary Motor and Sensory Neuropathy (Charcot-Marie-Tooth Disease)

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Pages 50-55 | Published online: 08 Jul 2009

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Belinda Buetti & Linda M. Luxon. (2014) Vestibular involvement in peripheral neuropathy: A review. International Journal of Audiology 53:6, pages 353-359.
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Jay Goswamy, Iain A Bruce, Kevin M J Green & Martin P O'Driscoll. (2012) Cochlear implantation in a patient with sensori-neural deafness secondary to Charcot−Marie−Tooth disease. Cochlear Implants International 13:3, pages 184-187.
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Articles from other publishers (23)

Anissa Rym Saidia, Jérôme Ruel, Amel Bahloul, Benjamin Chaix, Frédéric Venail & Jing Wang. (2023) Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder. Journal of Clinical Medicine 12:3, pages 738.
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J. E. Choi, H. Y. Seol, J. M. Seok, S. H. Hong, B.‐O. Choi & I. J. Moon. (2020) Psychoacoustics and neurophysiological auditory processing in patients with Charcot‐Marie‐Tooth disease types 1A and 2A. European Journal of Neurology 27:10, pages 2079-2088.
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Ji Eun Choi, Jin Myoung Seok, Jungmin Ahn, Yoon Sang Ji, Kyung Myun Lee, Sung Hwa Hong, Byung-Ok Choi & Il Joon Moon. (2018) Hidden hearing loss in patients with Charcot-Marie-Tooth disease type 1A. Scientific Reports 8:1.
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C. Lane Anzalone, Sarah Nuhanovic, Amy P. Olund & Matthew L. Carlson. (2018) Cochlear Implantation in Charcot-Marie-Tooth Disease: Case Report and Review of the Literature. Case Reports in Medicine 2018, pages 1-3.
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Petros V. Vlastarakos, Thomas P. Nikolopoulos, Evangelia Tavoulari, George Papacharalambous & Stavros Korres. (2008) Auditory neuropathy: Endocochlear lesion or temporal processing impairment? Implications for diagnosis and management. International Journal of Pediatric Otorhinolaryngology 72:8, pages 1135-1150.
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Rosalyn Davies. 2008. Scott-Brown's Otorhinolaryngology: Head and Neck Surgery 7Ed. Scott-Brown's Otorhinolaryngology: Head and Neck Surgery 7Ed 3837 3856 .
Dušan Butinar, Arnold Starr, Janez Zidar, Pantelitsa Koutsou & Kyproula Christodoulou. (2008) Auditory nerve is affected in one of two different point mutations of the neurofilament light gene. Clinical Neurophysiology 119:2, pages 367-375.
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Minh-Huong Cao-Nguyen, Maria-Izabel Kos & Jean-Philippe Guyot. (2007) Benefits and costs of universal hearing screening programme. International Journal of Pediatric Otorhinolaryngology 71:10, pages 1591-1595.
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Tetsuji Sekiya, Ken Kojima, Masahiro Matsumoto, Matthew C. Holley & Juichi Ito. (2007) REBUILDING LOST HEARING USING CELL TRANSPLANTATION. Neurosurgery 60:3, pages 417-433.
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W I. M Verhagen, P L. M Huygen, A A. W. M Gabreëls-Festen, M Engelhart, P J. W. B van Mierlo & B G. M van Engelen. (2005) Sensorineural Hearing Impairment in Patients with Pmp22 Duplication, Deletion, and Frameshift Mutations. Otology & Neurotology 26:3, pages 405-414.
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Karin Neijenhuis, Andy Beynon, Ad Snik, Baziel van Engelen & Paul van den Broek. (2003) Auditory Processing in Patients With Charcot-Marie-Tooth Disease Type 1A. Otology & Neurotology 24:6, pages 872-877.
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R Naito, T Murofushi, M Mizutani & K Kaga. (2003) Myelin-deficiency in the cochlear nerve of the ‘bt’ mutant hamster. Hearing Research 176:1-2, pages 17-24.
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Arthur Podwall, David Podwall, Toni G. Gordon, Paula Lamendola & Arnold P. Gold. (2016) Unilateral Auditory Neuropathy: Case Study. Journal of Child Neurology 17:4, pages 306-309.
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M.J. Kovach, K.C.M. Campbell, K. Herman, B. Waggoner, D. Gelber, L.F. Hughes & V.E. Kimonis. (2002) Anticipation in a unique family with Charcot‐Marie‐Tooth syndrome and deafness: Delineation of the clinical features and review of the literature. American Journal of Medical Genetics 108:4, pages 295-303.
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T. StojkovicP. LatourA. VandenbergheJ.F. HurteventP. Vermersch. (1999) Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q). Neurology 52:5, pages 1010-1010.
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Hiroshi Matsuoka, Kuang-Chuan Cheng, Yoshiro Yazawa, Marc S. Krug & Tai-June Yoo. (2016) Murine Model of Autoimmune Hearing Loss Induced by Myelin Protein P0. Annals of Otology, Rhinology & Laryngology 108:3, pages 255-264.
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G Nicholson & A Corbett. (1996) Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.. Journal of Neurology, Neurosurgery & Psychiatry 61:1, pages 43-46.
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Kendall Lisa Hanft & Joseph HaddadJr.Jr.. (1994) Progressive sensorineural hearing loss (SNHL) and peripheral neuropathy: a case report. International Journal of Pediatric Otorhinolaryngology 28:2-3, pages 229-234.
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O. Pinhas Hamiel, A. Raas-Rothschild, M. Upadhyaya, M. Frydman, I. Sarova-Pinhas, N. Brand & J.H. Passwell. (1993) Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: A new variant. The Journal of Pediatrics 123:3, pages 431-434.
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Jane E. Deal, Susan M. Hall, Richard A. C. Hughes & Susan P. A. Rigden. (1993) Alport's syndrome and hereditary motor and sensory neuropathy type I ? an unfortunate coincidence. Pediatric Nephrology 7:2, pages 156-158.
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V Scaioli, D Pareyson, G Avanzini & A Sghirlanzoni. (1992) F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.. Journal of Neurology, Neurosurgery & Psychiatry 55:11, pages 1027-1031.
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Natan Gadoth, Carlos R Gordon, Naomi Bleich & Hilel Pratt. (1991) Three modality evoked potentials in Charcot-Marie-Tooth disease (HMSN-1). Brain and Development 13:2, pages 91-94.
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Kristal Hagemoser, Joel Weinstein, George Bresnick, Robert Nellis, Susan Kirkpatrick & Richard M. Pauli. (2005) Optic atrophy, hearing loss, and peripheral neuropathy. American Journal of Medical Genetics 33:1, pages 61-65.
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