Vestibular involvement in peripheral neuropathy: A review

References

• Alper G. & Narayanan V. 2003. Friedreich's ataxia. Pediatr Neurol, 28, 335–341.
   PubMedGoogle Scholar
• Baloh R.W., Konrad H.R. & Honrubia V. 1975. Vestibulo-ocular function in patients with cerebellar atrophy. Neurology (Minneap), 25, 160–168.
   PubMed Web of Science ®Google Scholar
• Barohn R.J., Kissel J.T., Warmolts J.R. & Mendell J.R. 1989. Chronic inflammatory demyelinating polyradiculoneuropathy. Arch Neurol, 46, 878–884.
   PubMed Web of Science ®Google Scholar
• Bektas D., Gazioglu S., Arslan S., Cobanoglu B., Boz C. et al. 2008. VEMP responses are not affected in non-insulin-dependent diabetes mellitus patients with or without polyneuropathy. Acta Otolaryngol, 128, 768–71.
   PubMed Web of Science ®Google Scholar
• Berlin C. and Hood L. 2001. Auditory neuropathy (auditory desynchrony) disables efferent suppression of otoacoustic emissions. In: Y. Sininger & A. Starr (eds.), Auditory Neuropathy. San Diego: Sininger, p. 183.
   Google Scholar
• Bird T.D. & Griep E. 1981. Pattern reversal visual-evoked potentials. Studies in Charcot-Marie-Tooth hereditary neuropathy. Arch Neurol, 38, 739–741.
   PubMedGoogle Scholar
• Biurrun O., Ferrer J.P., Lorente J., Espana R., Gomis R. et al. 1991. Asymptomatic electronystagmographic abnormalities in patients with type I diabetes mellitus. ORL J Otorhinolaryngol Relat Spec, 53, 335–338.
   PubMed Web of Science ®Google Scholar
• Bittar R.S.M., Sanchez T.G., Santoro P.P. & Medeiros I.R.T. 1988. O metabolismo da glicose e o ouvido interno. Arq Otorrinolaringol, 2, 39–44.
   Google Scholar
• Bloem B.R., Visser J.E. & Carpenter M.G. 2001. Compensatory strategies in patients with longstanding balance impairment. In: J.C.E. Van de Burg, B.F. Fong, M.I.J. Hijl, R. Huys, M. Pijnappels, A.A. Post (eds.), Balance at All Times. Proceedings of the fifth symposium of the institute for fundamental and clinical human movement sciences. Amsterdam: IFKB, pp. 51–73.
   Google Scholar
• Brown K.E., Whitney S.L., Marchetti G.F., Wrisley D.M., Furman J.M. 2006. Physical therapy for central vestibular dysfunction. Arch Phys Med Rehabil, 87, 76–81.
   PubMed Web of Science ®Google Scholar
• Butinar D., Zidar J., Leonardis L., Popovic M., Kalaydjieva L. et al. 1999. Hereditary auditory, vestibular, motor, and sensory neuropathy in Slovenian Roma (Gypsy) kindred. Ann Neurol, 46, 366–44.
   PubMedGoogle Scholar
• Butinar D., Starr A. & Vatovec J. 2000. Brainstem auditory-evoked potentials and cochlear microphonics in the HMSN family with auditory neuropathy. Eur J Physiol, 439 (Suppl.), 204–205.
   Google Scholar
• Colvin I.B. 2006. Audiovestibular manifestations of sarcoidosis: A review of the literature. Laryngoscope, 116, 75–82.
   PubMedGoogle Scholar
• Dyck P.J., Lambert E.H. 1968. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy I: Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol, 18, 603–618.
   PubMed Web of Science ®Google Scholar
• Dyck P.J. 1984. Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory and autonomic neurons. In: P.J. Dyck, P.K. Thomas, E.H. Lambert, R. Bunge, (eds). Peripheral Neuropathy. Philadelphia: WB Sauders, pp. 1600–1655.
   Google Scholar
• Ell J., Prasher D. & Rudge P. 1984. Neuro-otological abnormalities in Friedreich's ataxia. J Neurol Neurosurg Psychiatry, 47, 26–32.
   PubMedGoogle Scholar
• Frohman E.M., Tusa R., Mark A.S. & Cornblath D.R. 1996. Vestibular dysfunction in chronic inflammatory demyelinating polyneuropathy. Ann Neurol, 39, 529–535.
   PubMedGoogle Scholar
• Fujikawa S. & Starr A. 2000. Vestibular neuropathy accompanying auditory and peripheral neuropathies. Arch Otolaryngol Head Neck Surg, 126, 1453–1456.
   PubMedGoogle Scholar
• Gawron W., Pospiech L., Orendorz-Fraczkowska K. & Noczynska A. 2002. Are there any disturbances in vestibular organ of children and young adults with type I diabetes?Diabetologia, 45, 728–734.
   PubMed Web of Science ®Google Scholar
• Hallpike C.S., Harriman D.G.F. & Wells C.E.C. 1980. A case of afferent neuropathy and deafness. J Laryngol Otol, 94, 945–964.
   PubMedGoogle Scholar
• Hanson P.A., Farber R.E. & Armstrong R.A. 1970. Distal muscle wasting, nephritis, and deafness. Neurology (Minneap), 20, 426–434.
   PubMedGoogle Scholar
• Harding A.E. & Thomas P.K. 1980. The clinical features of hereditary motor and sensory neuropathy type I and II. Brain, 103, 259–280.
   PubMed Web of Science ®Google Scholar
• Harrison R.V. 1998. An animal model of auditory neuropathy. Ear Hear, 19, 355–61.
   PubMed Web of Science ®Google Scholar
• Hayasaka K., Himoro M., Sato W., Takada G., Uyemura K. et al. 1993. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat Genet Sep, 5, 31–4.
   PubMed Web of Science ®Google Scholar
• Hooper R. & Holden H. 1970. Acoustic and vestibular problems in sarcoidosis. Arch Otolaryngol, 92, 386–391.
   PubMedGoogle Scholar
• Hughes J.T. & Brownwell B. 1972. Pathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease). J Neurol Neurosurg Psychiatry, 35, 648–657.
   PubMed Web of Science ®Google Scholar
• Hybels R.L. & Rice D.H. 1976. Neuro-otologic manifestations of sarcoidosis. Laryngoscope, 86, 1873–1878.
   PubMedGoogle Scholar
• Jacot E. & Wiener-Vacher S. 2008. Potential value of vestibular-evoked myogenic potentials in paediatric neuropathies. Journal of Vestibular Research, 18, 231–237.
   PubMedGoogle Scholar
• Jen J., Baloh R.H., Ishiyama A. & Baloh R.W. 2005. Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene. J Neurol Sci, 237, 21–24.
   PubMedGoogle Scholar
• Joo I.S., Ki C.S., Joo S.Y., Huh K. & Kim J.W. 2004. A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness. Neuromuscul Disord, 14, 325–328.
   PubMed Web of Science ®Google Scholar
• Khasanov S.A., Vasilyeva V.P. & Mazovetsky A.G. 1980. Vestibular function in the early forms of diabetes mellitus. Vestn Otorhinolaringol (pol), 6, 34–37.
   Google Scholar
• Kirkham T.H., Guitton D., Katsarkas A., Kline L.B. & Andermann E. 1979. Oculomotor abnormalities in Friedreich's ataxia. Can J Neurol Sci, 6, 167–172.
   PubMedGoogle Scholar
• Klagenberg K.F., Zeigelboim B.S., Jurkiewicz A.L. & Martins-Bassetto J. 2007. Vestibulocochlear manifestations in patients with type I diabetes mellitus. Rev Bras Otorhinolaringol, 73, 353–358.
   Google Scholar
• Kovach M.J., Lin J-P., Boyadjiev S., Campbell K.C., Mazzeo L. et al. 1999. A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness. Am J Hum Genet, 64, 1580–1593.
   PubMedGoogle Scholar
• Kovach M.J., Campbell K.C., Herman K., Waggoner B., Gelber D. et al. 2002. Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness. Delineation of the clinical features and review of the literature. Am J Med Genet, 108, 295–303.
   PubMed Web of Science ®Google Scholar
• Kowalski J.W., Rasheva M. & Zakrzewska B. 1991. Visual and brainstem auditory-evoked potentials in hereditary motor-sensory neuropathy. Electromyogr Clin Neurophysiol, 31, 167–172.
   PubMedGoogle Scholar
• Lemieux G. & Neemeh J.A. 1967. Charcot-Marie-Tooth disease and nephritis. Canad Med Ass J, 97, 1193–1198.
   PubMedGoogle Scholar
• Lopez-Diaz-de-Leon E., Silva-Rojas A., Ysunza A., Amavisca R. & Rivera R. 2003. Auditory neuropathy in Friedreich's ataxia. A report of two cases. Int J Pediatr Otorhinolaryngol, 67, 641–648.
   PubMedGoogle Scholar
• Lupski J.R., Jeffrey G., Gonzaga-Jauregui C., Rio Deiros D., Chen D.C.Y. et al. 2010. Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. N Engl J Med, 362, 1181–1191.
   PubMed Web of Science ®Google Scholar
• Majumdar B. & Crowther J. 1983. Hearing loss in sarcoidosis. J Laryngol Otol, 97, 635–639.
   PubMedGoogle Scholar
• Manchaiah V.K., Zhao F., Danesh A.A. & Duprey R. 2011. The genetic basis of auditory spectrum disorder (ANSD). Int J Pediatr Otorhinolaryngol, 75, 151–158.
   PubMed Web of Science ®Google Scholar
• McLeod J.G., Low P.A. & Morgan J.A. 1978. Charcot-Marie-Tooth disease with Leber optic atrophy. Neurology, 28, 179–184.
   PubMedGoogle Scholar
• McKusick V.A. 1998. Mendelian Inheritance in Man. Baltimore: Johns Hopkins University Press. Available at: www.ncbi.nlm.nih.gov/omim
   Google Scholar
• Melgaard B. & Zilstorff K. 1979. Central vestibular involvement in peroneal muscle atrophy: A preliminary report. Ann Neurol, 5, 118–120.
   PubMedGoogle Scholar
• Monday L.A., Lemieux B., St. Vincent H. & Barbeau A. 1978. Clinical and electronystagmographic findings in Friedreich's ataxia. Can J Neurol Sci, 5, 71–73.
   PubMedGoogle Scholar
• Musiek F.E., Weider D.J. & Mueller R.J. 1982. Audiologic findings in Charcot-Marie-Tooth disease. Arch Otolaryngol, 108, 595–599.
   PubMedGoogle Scholar
• Natout M.A.Y., Terr L.I., Linthicum F.H. & House W.F. 1987. Topography of vestibulocochlear nerve fibers in the posterior cranial fossa. Laryngoscope, 97, 954–958.
   PubMed Web of Science ®Google Scholar
• Neijenhuis K., Beynon A., Snik A., van Engelen B. & van der Broek P. 2003. Auditory processing in patients with Charcot-Marie-Tooth disease type 1A. Otol Neurotol, 24, 872–877.
   PubMedGoogle Scholar
• Ohtake T., Komori T., Hirose K. & Tanabe H. 1990. CNS involvement in Japanese patients with chronic inflammatory demyelinating polyradiculoneuropathy. Acta Neurol Scand, 81, 108–112.
   PubMed Web of Science ®Google Scholar
• Ormerod I.E.C., Waddy H.M. & Kermode A.G. et al. 1990. Involvement of the central nervous system in chronic inflammatory demyelinating polyneuropathy: A clinical, electrophysiological and magnetic resonance imaging study. J Neurol Neurosurg Psychiatry, 53, 789–793.
   PubMed Web of Science ®Google Scholar
• Palla A., Schmid-Priscoveanu A., Studer A., Hess K. & Straumann D. 2009. Deficient hight-acceleration vestibular function in patients with polyneuropathy. Neurology, 72, 2009–2013.
   PubMedGoogle Scholar
• Palop J.J., Chin J. & Mucke L. 2006. A network dysfunction perspective on neurodegenerative diseases. Nature, 443, 768–73.
   PubMed Web of Science ®Google Scholar
• Raeymaekers P., Timmerman V., Nelis E., De Jonghe P., Hoogendijk J.E. et al. 1991. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. Neuromuscul Disord, 1, 93–7.
   PubMedGoogle Scholar
• Raglan E., Prasher D.K., Trinder E. & Rudge P. 1987. Auditory function in hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Acta Otolaryngol, 103, 50–55.
   PubMed Web of Science ®Google Scholar
• Robertson N.G., Kheterpal U., Guierrez-Espeleta G.A., Bieber F.R. & Morton C.C. 1994. Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening. Genomics, 23, 42–50.
   PubMed Web of Science ®Google Scholar
• Salisachs P. 1976. Charcot-Marie-Tooth disease associated with essential tremor. J Neurol Sci, 28, 17–40.
   PubMedGoogle Scholar
• Salisachs P., Codina A., Gimenez Roldan S. & Zarranz J.J. 1979. Charcot-Marie-Tooth disease associated with essential tremor and normal and/or slightly diminished motor conduction velocity. Eur Neurol, 18, 49–58.
   PubMedGoogle Scholar
• Salisachs P. 1981. Unusual presentation of Charcot-Marie-Tooth disease. Inco-ordination with absent or minimal wasting. Report of two cases. J Neurol Sci, 50, 175–180.
   PubMedGoogle Scholar
• Salisachs P. 1982. Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease. J Neurol Neurosurg Psychiatry, 45, 1085–1091.
   PubMedGoogle Scholar
• Salvi R.J., Wang J., Ding D., Stecker N. & Arnold S. 1999. Auditory deprivation of the central auditory system resulting from selective inner hair cell loss: Animal model of auditory neuropathy. Scand Audiol Suppl, 51, 1–12.
   PubMedGoogle Scholar
• Samaha M. & Katsarkas A. 2000. Vestibular impairement in peripheral sensory neuropathies. J Otolaryngol, 29, 299–301.
   PubMedGoogle Scholar
• Sambuughin N., De Bantel A., McWilliams S. & Sivakumar K. 2003. Deafness and CMT disease associated with a novel four amino acid deletion in the PMP22 gene. Neurology, 60, 506–508.
   PubMed Web of Science ®Google Scholar
• Satya-Murti S., Cacace A.T. & Hanson P.A. 1979. Abnormal auditory-evoked potentials in hereditary motor-sensory neuropathy. Ann Neurol, 5, 445–459.
   PubMedGoogle Scholar
• Sazgar A.A., Yazdani N., Rezazadeh N. & Yazdi A.K. 2010. Vestibular evoked myogenic potential (VEMP) in patients with auditory neuropathy: Auditory neuropathy or audiovestibular neuropathy?Acta Otolaryngol, 130, 1130–1134.
   PubMed Web of Science ®Google Scholar
• Scaioli V., Pareyson D., Avanzini G. & Sghirlanzoni A. 1992. F response and somatosensory and brainstem auditory-evoked potential studies in HMSN type I and II. J Neurol Neurosurg Psychiatry, 55, 1027–1031.
   PubMed Web of Science ®Google Scholar
• Sheykholeslami K., Schmerber S., Habiby Kermany M. & Kaga K. 2005. Sacculo-collic pathway dysfunction accompanying auditory neuropathy. Acta Otolaryngol, 125, 786–791.
   PubMed Web of Science ®Google Scholar
• Smith T.L., Raynor E., Prazma J., Buenting J.E. & Pillsbury H.C. 1995. Insulino-dependent diabetic microangiopathy in the inner ear. J Laryngol Otol, 105, 236–240.
   Google Scholar
• Spoendlin H. 1974. I. Optic and cochleovestibular degenerations in hereditary ataxias. II.Temporal bone pathology in two cases of Friedreich's ataxia with vestibule-cochlear disorders. Brain, 97, 41–48.
   PubMedGoogle Scholar
• Starr A., Picton T.W., Sininger Y., Hood L.J. & Berlin C.I. 1996. Auditory neuropathy. Brain, 119, 741–753.
   PubMed Web of Science ®Google Scholar
• Starr A., Picton T.W. & Kim R. 2001a. Pathophysiology of auditory neuropathy. In: Y. Sininger, A. Starr (eds.), Auditory Neuropathy: A New Perspective on Hearing Disorders. San Diego: Singular, pp. 67–82.
   Google Scholar
• Starr A., Sininger Y., Nguyen T. et al. 2001b. Cochlear receptor (microphonic and summating potentials, otoacoustic emissions) and auditory pathway (auditory brain stem potentials) activity in auditory neuropathy. Ear Hear, 22, 91–9.
   PubMed Web of Science ®Google Scholar
• Torok N. 1976. Vestibular decruitment in central nervous system disease. Ann Otol Rhinol Laryngol, 85, 131–135.
   PubMed Web of Science ®Google Scholar
• Triantafyllou N., Rombos A., Athanasopoulou H., Siafakas A. & Malliara Larlakaki S. 1989. Electrophysiological study (EEG, VEPs, BAEPs) in patients with Charcot-Marie-Tooth (type HMSN I) disease. Electromyogr Clin Neurophysiol, 29, 259–263.
   PubMedGoogle Scholar
• Zingler V.C., Cnyrim C., Jahn K., Weintz E., Fernbacher J. et al. 2007. Causative factors and epidemiology of bilateral vestibulopathy in 255 patients. Ann Neurol, 61, 524–532.
   PubMed Web of Science ®Google Scholar