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Genetic Hearing Impairment: Its Clinical Presentations(61 Advances in Oto-Rhino-Laryngology)

Genetic Hearing Impairment: Its Clinical Presentations(61 Advances in Oto-Rhino-Laryngology)

          
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About the Book

A decade of innovative findings in the research of molecular biology of hearing and deafness is reflected in this volume. The genetic causes for many types of syndromic and non-syndromic deafness are identified and genotypic-phenotypic relationships are explored. Although the type and degree of deafness caused by mutations in different genes significantly overlap, relatively unique age-related audiometric profiles are also emerging. For example, the audioprofile of DFNA1 and DFNA6-14 is a low-frequency sensorineural hearing loss; with DFNA8-14 it is a mid-frequency sensorineural hearing loss, and with DFNA2, DFNA5 and DFNA20-26 it is a high-frequency progressive hearing loss. Recognizing such audioprofiles can facilitate well-guided decision-making in clinical practice and can direct genetic testing for deafness. With an accurate genetic diagnosis, prognostic information can be provided to patients and their families. In the future, gene-specific habilitation options may also become available. To keep up to date with new clinical standards of diagnosing genetic hearing impairment, this book is indispensable reading to otorhinolaryngologists and audiologists.


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Product Details
  • ISBN-13: 9783318008708
  • Publisher: S Karger Ag
  • Publisher Imprint: S Karger AG
  • Language: English
  • Series Title: 61 Advances in Oto-Rhino-Laryngology
  • ISBN-10: 3318008702
  • Publisher Date: 01 Jul 2002
  • Binding: Digital (delivered electronically)
  • No of Pages: 248
  • Sub Title: Its Clinical Presentations


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Genetic Hearing Impairment: Its Clinical Presentations(61 Advances in Oto-Rhino-Laryngology)
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