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This book deals with those disorders of the skeleton associated with known biochemical abnormalities of its components. It comprehensively covers common polygenic and rare monogenic disorders and emphasizes the new advances which have been made in bone cell biology and in human skeletal disease particularly as a result of molecular medicine. This has been achieved within an easily readable and well-illustrated book. It is written for the postgraduate and clinician who finds disorders of the skeleton mysterious and for whom an understandable explanation is not always available. It will be of particular interest to those who look after patients with a wide variety of metabolic bone diseases, including rheumatologists, endocrinologists and orthopedic surgeons, and contains new information of interest to pediatricians and geneticists. This branch of medicine is currently not well taught and even the experienced clinician may not have encountered some of these disorders.
This text investigates the intersection of biochemical abnormalities and skeletal disorders to provide a comprehensive framework for understanding human bone disease. The authors, Paul Wordsworth and Roger Smith, utilize recent advancements in molecular medicine and bone cell biology to clarify complex metabolic conditions. By bridging the gap between basic science and clinical practice, the book aims to demystify skeletal pathologies for medical professionals who encounter these rare and polygenic disorders in their daily practice.
What You Will Find
Scope Limits
Clinicians and postgraduates frequently cite this work as a necessary resource for navigating the complexities of metabolic bone disease. Experts highlight the text for its ability to synthesize dense molecular data into a format that remains accessible for practicing rheumatologists, endocrinologists, and geneticists.
Page Count:
470
Publication Date:
2005-04-21
Publisher:
Oxford University Press
ISBN-10:
0192617400
ISBN-13:
9780192617408
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