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OverviewThis book approaches the differential diagnosis and management of rare, hereditary cancer syndromes from a practical angle, addressing the issues pertinent to each tumour type as encountered by health professionals in their day-to-day practice. This book enables readers to correctly identify patients with rare cancer syndromes who would benefit from genetic counselling and testing, and provides the necessary knowledge for appropriate patient management and advising at-risk family members. It begins by describing recent advances in genetic testing for cancer-predisposing genes. Leading experts from Europe and Australia then offer detailed, up-to-date guidance on the diagnosis and management of a wide range of hereditary cancers. The concluding chapter examines the wider issues that are raised by genetic testing for rare cancer syndromes for patients, families and health professionals. This book is an invaluable source of information for all specialists involved in the care of suchpatients and their families. Full Product DetailsAuthor: Gabriella Pichert , Chris JacobsPublisher: Springer International Publishing AG Imprint: Springer International Publishing AG Edition: Softcover Reprint of the Original 1st 2016 ed. Volume: 205 Dimensions: Width: 15.50cm , Height: 1.30cm , Length: 23.50cm Weight: 3.869kg ISBN: 9783319807027ISBN 10: 3319807021 Pages: 238 Publication Date: 22 April 2018 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Manufactured on demand We will order this item for you from a manufactured on demand supplier. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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