This comprehensive guide to polycystic kidney disease captures the
growing knowledge of this common, potentially-fatal and hereditary
disease. The first two sections of the book provide an overview of
PKD gene structures, mutations and pathophysiologic mechanisms.
This is followed by chapters focused on PKD's clinical features,
including renal and extrarenal manifestations, and appropriate
management of patients. The final section covers current clinical
trials and emerging therapies in PKD. Authored by experts in the
field, this book provides the clinician and researcher with
critical information on basic and translational science and
clinical approaches in one concise resource.
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