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Genetics of Cerebrovascular Disease [Hardcover]

Mark Alberts (Editor)

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Book Description

January 15, 1999 0879935847 978-0879935849 1
This is the first book that focuses on genetics and stroke, an area of ever growing clinical and research importance. It integrates laboratory, applied and clinical research, with an emphasis on molecular genetic and genetic epidemiologic aspects of cerebrovascular disease.

Beginning with an overview of the key risk factors for stroke, most of the major stroke types and syndromes are detailed, as well as the key genetic advances for several stroke mechanisms and etiologies. The text also provides expert guidance for evaluating patients' genetic stroke profile. Extensive bibliographies for each chapter further guide the reader to topics of particular interest.

As the pioneering text on this topic, Genetics of Cerebrovascular Disease should be of considerable interest and value to both clinicians and researchers in this area.


Editorial Reviews

From The New England Journal of Medicine

Is stroke a genetic disease? Genetics of Cerebrovascular Disease puts forth the message that genetic factors do play a part in the pathogenesis of stroke. Traditionally, stroke has not been considered an inherited disease, and most cerebrovascular events are thought to be sporadic. However, there is considerable evidence supporting the view that cerebrovascular diseases are, in part, genetically determined. The chief risk factors for stroke, such as hypertension and diabetes, have a genetic component, and certain familial diseases affecting blood vessels or blood clotting are associated with an increased incidence of cerebrovascular events. The application of molecular genetic techniques to the study of cerebrovascular diseases and their risk factors has led to a wealth of information on the contribution of genetic factors to cerebrovascular disorders. Genetics of Cerebrovascular Disease provides, for the first time, a synopsis of such evidence in a series of competently written chapters by experts in the field.

Appropriately, the book begins with an outline of genetic principles and techniques. This section, especially the readable and informative first chapter, provides an excellent introduction to some of the subsequent chapters. The next section examines the genetics of risk factors for cerebrovascular disease. This section, which provides a detailed review of the genetics of hypertension, lipid metabolism, atherosclerosis, and coagulation disorders, is likely to appeal more to readers with a specific interest in these topics than to other readers. The seven chapters in the third section focus on the genetics of specific causes of stroke and stroke syndromes. This section, the heart of the book, deals with the genetics of vasculopathies, vascular malformations, intracranial aneurysms, and systemic diseases associated with stroke. A chapter on pediatric stroke is included. These chapters are uniformly excellent and provide up-to-date and detailed coverage of the respective topics. It is surprising, however, that vasculitis and connective-tissue disease are not dealt with in greater detail. The last section of the book focuses on practical issues concerning the evaluation of patients for inherited causes of stroke and genetic counseling. The final chapter, on gene therapy, reviews the methods of gene transfer and lists the diseases in which gene therapy might be useful. The material presented, however, has few practical implications, at least for the time being.

Overall, this useful book provides the specialist and the general reader with an extensive and up-to-date review of genetic factors that may play a part in cerebrovascular diseases. The chapters are packed with information and have been written clearly. The book is an excellent resource for physicians dealing with cases of cerebrovascular diseases in which the family history suggests the role of inheritance. The citations are numerous and current, not uncommonly including contributions published in the late 1990s. The figures are generally clear and, although not lavish, make the point intended. Some aspects of the book could have been improved. For example, a glossary of terms would have helped the less informed reader with sections in which molecular genetic terms are used frequently. In addition, redundant information in the many chapters dealing with risk factors and coagulation disorders could have been eliminated. However, these are relatively minor shortcomings that could easily be rectified in future editions of the book. On the whole, this book fills an obvious gap in the field and is therefore a welcome addition to the neurologic and general medical literature.

Reviewed by Costantino Iadecola, M.D.
Copyright © 1999 Massachusetts Medical Society. All rights reserved. The New England Journal of Medicine is a registered trademark of the MMS.

Review

Overall, this useful book provides the specialist and the general reader with an extensive and up-to-date review of genetic factors that may play a part in cerebrovascular diseases. The chapters are packed with information and have been written clearly. The book is an excellent resource for physicians dealing with cases of cerebrovascular diseases in which the family history suggests the role of inheritance. ...On a whole, this book fills an obvious gap in the field and is therefore a welcome addition to the neurologic and general medical literature."

--The New England Journal of Medicine


"The audience identified in the preface is both practitioners and researchers. I believe that there is something to be gained from this work for both groups. The editor is certainly reputable in the field and respected.
"I enjoyed reading and reviewing this book."

--Doody’s Review Service


"The broad overview provided together with a comprehensive reference list makes this book a valuable addition to the bookshelf of the neurologist caring for young stroke patients or those with unusual stroke syndromes. Although this is a rapidly evolving field, little of what is contained in this book will necessarily go out of date. Rather it will act as a firm base to which future developments will be added."

--Brain


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Inside This Book (learn more)
First Sentence:
This chapter will review the basic genetic concepts and molecular genetic techniques that are used for the study of human diseases. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
pediatric stroke, familial stroke, mitochondrial angiopathy, familial intracranial aneurysms, moyamoya disease, renin gene, lesterol acyltransferase, lagen gene, tracerebral hemorrhage, tiphospholipid antibodies, cervical artery dissections, chemic stroke, hereditary cerebral hemorrhage, pathogenic genes, childhood stroke, genetic counseling process, neonatal purpura fulminans, nonfamilial cases, procoagulant response, cerebral amyloid angiopathy, acyltransferase deficiency, sential hypertension, collagen deficiency, glycoprotein syndrome, angiotensinogen gene
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Hum Genet, Biol Chem, Proc Natl Acad Sci, New York, Clin Invest, Ann Neurol, Arch Neurol, Thromb Haemost, Lipid Res, Nat Genet, Genetic Causes of Pediatric Stroke, Med Genet, Hum Gene Ther, Ann Intern Med, Biochem Biophys Res Commun, Molecular Genetics of Lipid Metabolism, Futura Publishing Company, Neurol Sci, Churchill Livingstone, Clin Genet, Genetics of Coagulation Disorders, Family Studies of Stroke, Hum Mol Genet, Child Neurol, Neurol Neurosurg Psychiatry
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