3rd edition. — Oxford University Press, 2013. — 749 p. — ISBN: 9780199731961
This is the third edition of the foremost medical reference on hereditary hearing loss. Chapters on epidemiology, embryology, non-syndromic hearing loss, and syndromic forms of hearing loss have all been updated with particular attention to the vast amount of new information on molecular mechanisms, and chapters on clinical and molecular diagnosis and on genetic susceptibility to ototoxic factors have been added. As in previous editions, the syndromes are grouped by system (visual, metabolic, cardiologic, neurologic, musculoskeletal, endocrine, etc.), with each chapter written by a recognized expert in the field. Written for practicing clinicians, this volume is an excellent reference for physicians, audiologists, and other professionals working with individuals with hearing loss and their families, and can also serve as a text for clinical training programs and for researchers in the hearing sciences.
Genetic Hearing Loss: A Brief History
Epidemiology, Etiology, Genetic Mechanisms, and Genetic Counseling
Embryology of the Mammalian Ear
Gene/Environment Interactions in Acquired Hearing Loss
Syndrome Diagnosis and Investigation in the Hearing-impaired Patient
Genetic Hearing Loss with No Associated Abnormities
Genetic Hearing Loss Associated with External Ear Abnormalities
Eye Disorders
Genetic Hearing Loss Associated with Musculoskeletal Disorders
Genetic Hearing Loss Associated with Renal Disorders
Genetic Hearing Loss Associated with Neurologic and Neuromuscular Disorders
Genetics Hearing Loss Associated with Cardiac Abnormalities
Genetic Hearing Loss Associated with Endocrine Disorders
Genetic Hearing Loss Associated with Metabolic Disorders
Integumentary Disorders
Oral and Dental Disorders
Chromosome Disorders