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English
Oxford University Press
21 March 1996
Many inherited diseases and non-hereditary disorders have in common the development of renal cystic disease.

The most common, autosonal dominant polycystic kidney disease, is responsible for 5-10% of end-stage renal failure treated by dialysis or transplantation.

Since the publication six years ago of the last book on polycystic kidney disease, a number of genes causing the disease have been identified, mapped, or sequenced; new experimental models and the application of molecular biology techniques have provided new insights into the pathogenesis R

polycystic kidney disease; novel clinical studies have provided valuable information for the prevention, evaluation, and treatment of the complications of this disease.

This book provides an updated, state-of-the-art review of the genetics, pathophysiology, evaluation, and management of these diseases and will be of interest to both basic researchers and clinicians in nephrology.

Edited by:   , , , ,
Imprint:   Oxford University Press
Country of Publication:   United Kingdom
Dimensions:   Height: 248mm,  Width: 174mm,  Spine: 38mm
Weight:   1g
ISBN:   9780192625786
ISBN 10:   0192625780
Series:   Oxford Clinical Nephrology Series
Pages:   606
Publication Date:  
Audience:   Professional and scholarly ,  Undergraduate
Format:   Hardback
Publisher's Status:   Active
Part I: Cystic renal disease: experimental models and pathology 1: Principles of molecular biology as applied to the study of disease 2: In vitro models in the study of renal cystogenesis 3: Mouse models of polycystic kidney disease 4: In vivo models in non-murine species 5: Pathogenesis of polycystic kidney disease: basement membrane and extracellular matric 6: Pathogenesis of polycystic kidney disease: altered cellular function Part II: Cystic renal disease: clinical spectrum 7: Classification of cystic kidneys 8: Diagnostic imaging of renal cystic diseases 9: Autosomal recessive polycystic kidney disease: clinical and genetic profiles 10: Acquired renal cystic disease 11: Tuberous sclerosis complex 12: Von Hippel-Lindau Disease Part III: Adult polycystic kidney disease: natural history and genetics 13: Definition and natural history of autosomal dominant polycystic kidney disease 14: Cloning strategies and genetics of type 1 autosomal dominant polycystic kidney disease Part IV: Adult polycystic kidney disease: clinical features 16: Hypertension in polycystic kidney disease 17: Progression to renal insufficiency 18: Management of end-stage renal failure and problems of transplantation in autosomal dominant polycystic kidney disease 19: Chronic pain and its medical and surgical management in renal cystic disease Part V: Adult polycystic kidney disease: complications 20: Miscellaneous renal and systemic complications of autosomal dominant polycystic kidney disease including infection 21: Polycystic liver disease 22: Intracranial aneurysms in autosomal dominant polycystic kidney disease 23: Particular problems in childhood and adolescents in autosomal dominant polycystic kidney disease 24: Counselling and ethical considerations in autosomal polycystic kidney disease

Reviews for Polycystic Kidney Disease

This is a further addition to the 'Oxford Clinical Nephrology' Series and provides an extensive review of our current knowledge on polycystic kidney disease...Overall this is an excellent book and provides much useful information for both the diagnosis and management of renal cystic diseases. It can be highly recommended, not just for the outstanding way the subject has been approached, but because the book also contains useful background information which greatly enhances the overall value. * Nephrol Dial Transplant, 1998, 13: 1904-1908 * I found this book a delight to read - it provides a balanced diet of genetics, pathophysiology and clinical medicine. For experts and researchers in the field there is detailed information and stimulation; for interested clinicians, the scientific sections are intelligibly presented and the clinical sections should be a real aid in day-to-day practice ... this book should be of wide interest. This book does not simply give a list of known features or research in the condition it covers, it also squarely addresses some of the more difficult problems which face clinicians and their patients. * Terry Feest, Journal of the Royal College of Physicians of London, Vol. 32, No. 1 January/February 1998 * I found this book a delight to read - it provides a balanced diet of genetics, pathophysiology and clinical medicine. For experts and researchers in the field there is detailed information and stimulation; for interested clinicians, the scientific sections are intelligibly presented and the clinical sections should be a real aid in day-to-day practice. This book does not simply give a list of known features or research in the condition it covers, it also squarely addresses some of the more difficult problems which face clinicians and their patients. * Terry Feest, Southmead Hospital, Journal of the Royal College of Physicians of London, Vol. 32, No. 1 January./February 1998 * a multi-authored, comprehensive review of the hereditary cystic kidney diseases ... There is useful information on virtually every page ... the book is well organized and well referenced, with figures and graphs that clearly augment the written text ... This text makes a useful addition to the clinician's library. * Bruce Z. Morgenstern, Pediatr Nephrol (1997) 11:664 *


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