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" Genetic hearing loss / "
edited by Patrick J. Willems
Document Type
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BL
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Record Number
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637557
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Doc. No
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dltt
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Title & Author
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Genetic hearing loss /\ edited by Patrick J. Willems
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Page. NO
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xiv, 483 pages :: illustrations ;; 24 cm
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ISBN
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0824743091
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: 9780824743093
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Bibliographies/Indexes
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Includes bibliographical references and index
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Contents
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Part I. Hearing and Hearing Loss -- 1. Normal Development of the Ear in the Human and Mouse / Lina M. Mullen, Yan Li, and Allen F. Ryan -- 2. Audiometric Tests and Diagnostic Workup / Paul J. Govaerts -- 3. Classification and Epidemiology / Alessandro Martini and Patrizia Trevisi -- Part II. Syndromic Hearing Loss -- 4. Usher Syndrome / William J. Kimberling -- 5. Pendred Syndrome / Shannon P. Pryor [and others] -- 6. Waardenburg Syndrome / Andrew P. Read -- 7. Jervell and Lange-Nielsen Syndrome / Lisbeth Tranebjaerg -- 8. HDR Syndrome / Hilde Van Esch and Koenraad Devriendt -- 9. Branchio-oto-renal Syndrome / Shrawan Kumar -- 10. Treacher Collins Syndrome / Jill Dixon and Michael J. Dixon -- 11. MYH9 / Anil K. Lalwani and Anand N. Mhatre -- 12. Mitochondrial Hearing Loss / Nathan Fischel-Ghodsian -- Part III. Genes Responsible for Nonsyndromic Hearing Loss -- 13. Gene Localization and Isolation in Nonsyndromic Hearing Loss / Patrick J. Willems -- 14. Connexins / Paolo Gasparini -- 15. Myosin VI / Nadav Ahituv [and others] -- 16. K+ Channel Gene KCNQ4 / Paul Coucke and Patrick J. Willems -- 17. COL11A2 257 / Wyman T. McGuirt, Guy Van Camp, and Richard J.H. Smith -- 18. POU-Domain Transcription Factors / Ronna Hertzano and Karen B. Avraham -- 19. [alpha]-Tectorin / P. Kevin Legan [and others] -- 20. EYA4 / Sigrid Wayne [and others] -- 21. DFNA 5 / Lut Van Laer, Egbert H. Huizing, and Guy Van Camp -- 22. COCH / Nahid G. Robertson and Cynthia C. Morton -- 23. Diaphanous / Kelly N. Owens and Mary-Claire King -- 24. Claudin 14 / Tamar Ben-Yosef, Edward R. Wilcox, and Thomas B. Friedman -- 25. CDH23 / Julie M. Schultz [and others] -- 26. TMPRSS3 / Stylianos E. Antonarakis and Hamish S. Scott -- 27. Otosclerosis / Kris Van Den Bogaert, Richard J.H. Smith, and Guy Van Camp -- Part IV. Miscellaneous Factors -- 28. Mechanisms that Regulate Hair Cell Differentiation and Regeneration / Brigitte Malgrange [and others] -- 29. Genetic Testing : Possibilities and Attitudes / Tim Hutchin, Karen Thompson, and Robert Mueller
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Abstract
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Describes the normal development of the ear; updates the classification and epidemiology of hearing loss; surveys the usage of audiometric tests and diagnostic medical examinations; illuminates the most important syndromes associated with hearing loss such as Usher, Pendred, and Waardenburg syndromes; discusses the maternal inheritance patterns of mitochondrial hearing loss; provides a roadmap to gene localization and isolation in nonsyndromic hearing loss, exploring connexins, tectorins, myosins, ion channels, and other disease genes; highlights otosclerosis, one of the most common types of hearing loss; considers mechanisms regulating hair cell differentiation and regeneration; and elucidates the future of genetic testing for hearing loss
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Subject
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Deafness-- Genetic aspects
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Subject
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Hearing Loss-- congenital
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Subject
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Hearing Loss-- genetics
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Subject
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Ear-- abnormalities
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Subject
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Molecular Biology
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Dewey Classification
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617.8/042
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LC Classification
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RF292.G455 2004
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NLM classification
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2003 N-996
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WV 270G32683 2004
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Added Entry
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Willems, Patrick J.,1956-
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