Comprehensive Guide to Wilson Disease: Causes, Diagnosis, and Treatment

Wilson Disease is an inherited genetic disorder that has devastating consequences for both the liver and neurologic/psychiatric health. It is of increasing interest to neurologists, hepatologists, and geneticists. When diagnosed early, it is treatable, and patients can live normal lives.

Molecular Pathophysiology of Wilson Disease

This volume describes the molecular pathophysiology of WD and the clinical and pathological effects of copper. Separate sections address both diagnosis and medical and surgical approaches to treatment.

Diagnosis and Treatment of Wilson Disease

Both adult and pediatric perspectives on diagnosis and treatment are addressed, and a section on genetics highlights advances in molecular diagnostics. Patient support groups that can aid in coping with this disease are also discussed, as are animal models for those interested in basic research on cell biology, pathophysiology, and treatment.

Expert Coverage and Perspectives

Edited work with chapters authored by leaders in the field from around the globe, providing the broadest, most expert coverage available.

Product Details

Series: Handbook of Clinical Neurology (Book 142) Hardcover: 264 pages Publisher: Elsevier; 1 edition (May 24, 2017) Language: English ISBN-10: 0444636250 ISBN-13: 978-0444636256 Product Dimensions: 7.5 x 0.8 x 10.2 inches