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Springer Molecular Diagnosis of Deafness - Modern Otology & Neurotology

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Description

This comprehensive medical reference explores the molecular diagnosis of deafness with emphasis on gene identification and clinical applications in modern otology and neurotology. The volume provides clinicians and researchers with detailed insights into the genetic underpinnings of hearing loss, covering genetic epidemiology of deafness genes, non-syndromic and syndromic hearing loss presentations, and the role of genetic testing in cochlear implantation planning. Chapters examine critical genes including GJB2, SLC26A4, and MYO7A with detailed molecular analysis, offering practical guidance on genetic testing methodologies and patient counselling strategies. Readers will discover how advances in molecular diagnostics are transforming clinical practice and enabling personalized treatment approaches for patients with hereditary hearing impairment across diverse populations.

Key Features

Springer publication covering molecular diagnosis of deafness with clinical application focus for otology and neurotology professionals.

Detailed analysis of major deafness genes including GJB2, SLC26A4, and MYO7A with their molecular mechanisms and clinical significance.

Comprehensive coverage of genetic epidemiology, non-syndromic hearing loss, and syndromic presentations in deafness diagnosis.

Practical guidance on genetic testing methodologies and patient counselling for hereditary hearing loss management.

Exploration of genetic testing's role in cochlear implantation selection and treatment planning for hearing-impaired patients.

Product Specifications

Format
hardcover
Domain
Amazon UK
Release Date
05 December 2025
Listed Since
27 September 2025

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