Autosomal Dominant Non-syndromal Low-frequency Sensorineural Hearing Impairment Linked to Chromosome 4p16 (DFNA14): Statistical Analysis of Hearing Threshold in Relation to Age and Evaluation of Vestibulo-ocular Functions

References

• Morton N E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci 1991; 630: 16–31
   PubMed Web of Science ®Google Scholar
• Marazita M L, Ploughman L M, Rawlings B, Remington E, Arnos K S, Nance W E. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population. Am J Med Genet 1993; 46: 486–91
   PubMed Web of Science ®Google Scholar
• Liu X, Xu L. Nonsyndromic hearing loss: an analysis of audiograms. Ann Otol Rhinol Laryngol 1994; 103: 428–33
   PubMed Web of Science ®Google Scholar
• Van Camp G, Willems P J, Smith R JH. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 1997; 60: 758–64
   PubMed Web of Science ®Google Scholar
• Van Camp G, Smith R JH. Hereditary Hearing Loss Homepage. 1998, World Wide Web URL: http://www.dnalab-www.uia.ac.be/dnalab/hhh
   Google Scholar
• León P E, Bonilla J A, Sánchez Al. Low frequency hereditary deafness in man with childhood onset. Am J Hum Genet 1981; 33: 209–14
   PubMed Web of Science ®Google Scholar
• León P E, Raventos H, Lynch E, Morrow J, King M-C. The gene for an inherited form of deafness maps to chromosome 5q31. Proc Natl Acad Sci USA 1992; 89: 5181–4
   PubMed Web of Science ®Google Scholar
• Coucke P, Van Camp G, Djoyodiharjo B, et al. Linkage of autosomal dominant hearing loss to tile short arm of chromosome 1 in two families. N Engl J Med 1994; 331: 425–31
   PubMed Web of Science ®Google Scholar
• Djelantik B. Progressive autosomal dominant hearing loss due to a genetic defect on chromosome 1 in families from West Java, An audiologic and genetic study. PhD Thesis 1996, Antwerp, Belgium
   Google Scholar
• Marres H, Van Ewijk M, Huygen P, et al. Inherited nonsyndromic hearing loss. An audio-vestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2. Arch Otolaryngol Head Neck Surg 1997; 123: 573–7
   PubMed Web of Science ®Google Scholar
• Kunst H, Marres H, Huygen P, et al. Nonsyndromic autosomal dominant progressive sensorineural hearing loss: Audiologic analysis of a pedigree linked to DFNA2. Laryngoscope 1998; 108: 74–80
   PubMed Web of Science ®Google Scholar
• Huizing E H, Van Bolhuis A H, Odenthal D W. Studies on progressive hereditary perceptive deafness in a family of 335 members. I. Genetical and general audiological results. Acta Otolaryngol 1966; 61: 35–41
   PubMedGoogle Scholar
• Huizing E H, Van Bolhuis A H, Odenthal D W. Studies on progressive hereditary perceptive deafness in a family of 335 members. II. Characteristic pattern of hearing deterioration. Acta Otolaryngol 1966; 61: 161–7
   PubMedGoogle Scholar
• Huizing E H, Van Bolhuis A H, Odenthal D W. Results of further studies on progressive hereditary sensorineural hearing loss. Audiology 1972; 12: 261–3
   Google Scholar
• Huizing E H, Van den Wijngaart W SIM, Verschuure J. A follow-up study of a family with dominant progressive inner ear deafness. Acta Otolaryngol 1983; 95: 620–6
   PubMed Web of Science ®Google Scholar
• Van den Wijngaart W SIM. Dominant erfelijke progressieve binnenoorslechthorendheid. 1982, PhD Thesis, Rotterdam, the Netherlands
   Google Scholar
• Van den Wijngaart W SIM, Huizing E H, Niermeijer M F, Verschuure J, Brocaar M P, Blom W. Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. I. Analysis of hearing deterioration. Audiology 1985; 24: 233–40
   PubMedGoogle Scholar
• Van den Wijngaart W SIM, Huizing E H, Niermeijer M F, Verschuure J, Brocaar M P, Blom W. Follow-up study in a family with dominant progressive hereditary sensorineural hearing impairment. II. Clinical aspects. Audiology 1985; 24: 336–42
   PubMed Web of Science ®Google Scholar
• Van Camp G, Coucke P, Dalemans W, et al. Localizations of a locus for non-syndromic hearing loss (DFNA5) to chromosome 7p. Hum Mol Genet 1995; 4: 2159–63
   PubMed Web of Science ®Google Scholar
• The Vanderbilt University Hereditary Deafness Study Group. Dominantly inherited low-frequency hearing loss. Arch Otolaryngol 1968; 88: 242–50
   PubMed Web of Science ®Google Scholar
• Hall J W, III, Bess F, Strouse A, Chase P. Dominant inherited low frequency hearing loss: documentation in five generations. XXII International Congress of Audiology. Halifax, Nova Scotia, Canada. July 3-8. 1994; 102, Book of abstracts p
   Google Scholar
• Lesperance M M, Hall J W, Bess F H, et al. A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4pl6.3. Hum Mol Genet 1995; 4: 1967–72
   PubMed Web of Science ®Google Scholar
• Kunst H, Marres H, Van Camp G, Cremers C. Review of non-syndromic autosomal dominant sensorineural hearing loss: a new field of research. Clin Otolaryngol 1998; 23: 9–17
   PubMedGoogle Scholar
• European Work Group on Genetics of Hearing Impairment. Infoletter 2. 1996, November
   Google Scholar
• International Organization for Standardization. ISO 389. Acoustics: Standard Reference Zero for the Calibration of Pure Tone Air Conduction Audiometers. Switzerland, International Organization for Standardization, Geneva 1985
   Google Scholar
• International Organization for Standardization. ISO 8253-1. Acoustics: Audiometric Test Methods, I: Basic Pure Tone Air and Bone Conduction Threshold Audiometry. Switzerland, International Organization for Standardization, Geneva 1989
   Google Scholar
• International Organisation for Standardization. ISO 7029. Acoustics–Threshold of hearing by air conduction as a function of age and sex for otologically normal persons. Switzerland, International Organization for Standardization, Geneva 1984
   Google Scholar
• Robinson D W, Sutton G J. Age effect in hearing–a comparative analysis of published threshold data. Audiology 1979; 18: 320–34
   PubMedGoogle Scholar
• Verhagen W IM, Ter Bruggen J P, Huygen P LM. Oculomotor, auditory, and vestibular responses in myotonic dystrophy. Arch Neurol 1992; 49: 954–60
   PubMedGoogle Scholar
• Theunissen E JJM, Huygen P LM, Folgering H T. Vestibular hyperreactivity and hyperventilation. Clin Otolaryngol 1986; 11: 161–9
   PubMed Web of Science ®Google Scholar
• Casselman J W, Kuhweide R, Deimling M, Ampe W, Dehaene I, Meeus L. Constructive interference in steady state (CISS)-3D FT MR imaging of the inner ear and cerebellopontine angle. Am J Neuroradiol 1993; 14: 47–57
   PubMed Web of Science ®Google Scholar
• Leigh R J, Zee D S. The Neurology of Eye Movements, 2nd ed. Davis, Philadelphia 1991
   Google Scholar