Rare hereditary cancers : diagnosis and management /

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Bibliographic Details
Imprint:[Cham] : Springer, 2016.
Description:1 online resource
Language:English
Series:Recent results in cancer research ; volume 205
Recent results in cancer research ; volume 205.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11254734
Hidden Bibliographic Details
Other authors / contributors:Pichert, Gabriella, editor.
Jacobs, Chris (Consultant genetic counsellor), editor.
ISBN:9783319299983
3319299980
3319299964
9783319299969
9783319299969
Digital file characteristics:text file
PDF
Notes:Includes bibliographical references and index.
English.
Online resource; title from PDF title page (EBSCO, viewed April 19, 2016).
Summary:This 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 such patients and their families.
Other form:Printed edition: 9783319299969
Standard no.:10.1007/978-3-319-29998-3