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Third edition
I. G. Joe Mayhew
Massey University
Palmerston North, NZ
Robert J. MacKay
University of Florida
Gainesville, Florida, USA
This edition first published 2022 © 2022 John Wiley & Sons Ltd
Edition History John Wiley & Sons Ltd (2e, 2008), Lea & Febiger (1e, 1989)
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Library of Congress Cataloging‐in‐Publication Data applied for [HB ISBN: 9781119477037]
Cover Design: Wiley
Cover Images: Courtesy of Quentin Roper, Courtesy of Joe Mayhew
For this third edition of Large Animal Neurology , we have enlisted Rob MacKay as coauthor to help us keep up with current trends and to maintain a reasonably worldwide—albeit somewhat Anglosphere—perspective.
As with previous editions, the general structure of the book consists of three parts. Part I( Chapters 1– 4) covers the background disciplines required for the evaluation of neurologic cases; Part II( Chapters 5– 30) provides concise overviews of the commonly encountered, major clinical presenting scenarios; and Part III( Chapters 31– 38) offers an extensively resourced discourse of most neurologic diseases of domestic large animals following an etiologic category. Readers thus can approach the text with a view to updating their evaluation of suspected clinical neurologic patients ( Part I), with a specific clinical syndrome in mind ( Part II), or to delve into details on most of the specific neurologic diseases of large domestic animals ( Part III).
Since the second edition of 2008, genetics and modern imaging techniques, in particular, have had a major impact on large animal neurology. Despite their profound utility, these diagnostic tests are not perfect. Thus, even dramatic and clearly defined changes seen on an MR or a CT image of a patient with a neurologic syndrome does not always indicate cause and effect. Likewise, as our genetic modeling of many diseases unravels, particularly of those with complex genetic characteristics, identifying a genetic association with a particular disorder does not mean that the patient’s signs are due solely to that inborn—or even acquired—genetic fingerprint. Therefore, as with all diagnostic ancillary aids we use, the results must be taken in conjunction with the results of repeated examinations to help formulate the most appropriate diagnostic and therapeutic plans. It also must be considered before undertaking any test, whether the results, considering their margin of error, will inform clinical management to a degree that benefit outweighs risk and cost. Otherwise, we might be better off not undertaking them.
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