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Titlebook: Rare Hereditary Cancers; Diagnosis and Manage Gabriella Pichert,Chris Jacobs Book 2016 Springer International Publishing Switzerland 2016 C

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發(fā)表于 2025-3-21 18:04:38 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Rare Hereditary Cancers
副標(biāo)題Diagnosis and Manage
編輯Gabriella Pichert,Chris Jacobs
視頻videohttp://file.papertrans.cn/822/821256/821256.mp4
概述Provides health professionals with up-to-date information on rare inheritable cancer syndromes.Offers clear, practical guidance on differential diagnosis and management.Covers a wide range of cancer t
叢書名稱Recent Results in Cancer Research
圖書封面Titlebook: Rare Hereditary Cancers; Diagnosis and Manage Gabriella Pichert,Chris Jacobs Book 2016 Springer International Publishing Switzerland 2016 C
描述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 suchpatients and their families..
出版日期Book 2016
關(guān)鍵詞Cancer Risks; Differential Diagnosis; Family History of Cancer; Genetic Tests; Management Options; Rare H
版次1
doihttps://doi.org/10.1007/978-3-319-29998-3
isbn_softcover978-3-319-80702-7
isbn_ebook978-3-319-29998-3Series ISSN 0080-0015 Series E-ISSN 2197-6767
issn_series 0080-0015
copyrightSpringer International Publishing Switzerland 2016
The information of publication is updating

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Diagnosis and Management of Hereditary Gastric Cancer, interpretation which require a high degree of selective expertise. Much of the remaining heritable risk of GC may be accounted for by low- and intermediate-penetrant genetic factors, i.e. common and rare variants, respectively. The advent of new methods such as next-generation sequencing has revealed a number of new candidate gene loci.
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Diagnosis and Management of Hereditary Sarcoma,ial fraction of sarcoma patients will be identified as carriers of known risk alleles. The translation of this knowledge into effective risk management programs and cancer treatments will be essential to changes in routine clinical practice.
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Diagnosis and Management of Hereditary Thyroid Cancer,y thyroid cancer (FNMTC) comprises about 5–15?% of NMTC and is a heterogeneous group of diseases, including both non-syndromic and syndromic forms. Non-syndromic FNMTC tends to manifest papillary thyroid carcinoma, usually multifocal and bilateral. Several high-penetrance genes for FNMTC have been i
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Diagnosis and Management of Hereditary Gastric Cancer,argely unknown. The risk associated with having one first-degree relative (FDR) with GC is approximately 1.3–3.5?fold increased. Hereditary cancer syndromes have been relatively well characterised, but their rarity largely precludes the development of trials of surveillance. In hereditary diffuse ga
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