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Rare hereditary cancers[electronic resource] :diagnosis and management /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	616.994042
書名/作者:	Rare hereditary cancers : diagnosis and management // edited by Gabriella Pichert, Chris Jacobs.
其他作者:	Pichert, Gabriella.
出版者:	Cham : : Springer International Publishing :, 2016.
面頁冊數:	xiv, 238 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Cancer - Genetic aspects.
標題:	Cancer - Diagnosis.
標題:	Cancer - Treatment.
標題:	Medicine & Public Health.
標題:	Oncology.
標題:	Human Genetics.
標題:	Cancer Research.
標題:	Nursing.
ISBN:	9783319299983
ISBN:	9783319299969
內容註:	Advances in genetic testing for cancer predisposing genes -- Diagnosis and management of inheritable pheochromocytomas and paragangliomas -- Diagnosis and management of inheritable kidney cancer syndromes -- Diagnosis and management of inheritable pancreatic cancers/melanomas -- Diagnosis and management of inheritable basal cell skin cancer syndromes -- Diagnosis and management of inheritable adrenal cancers -- Diagnosis and management of inheritable thyroid cancers -- Diagnosis and management of inheritable meningiomas/acoustic neuroma -- Diagnosis and management of inheritable gastric cancer syndromes -- Diagnosis and management of inheritable carcinoid syndromes -- Diagnosis and management of inheritable sarcoma syndromes -- Genetic testing for rare cancer syndromes: the wider issues for patients, families and health professionals.
摘要、提要註:	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.
電子資源:	http://dx.doi.org/10.1007/978-3-319-29998-3

Rare hereditary cancers[electronic resource] :diagnosis and management /
Rare hereditary cancersdiagnosis and management /[electronic resource] :edited by Gabriella Pichert, Chris Jacobs. - Cham :Springer International Publishing :2016. - xiv, 238 p. :ill., digital ;24 cm. - Recent results in cancer research,v.2050080-0015 ;. - Recent results in cancer research ;v.192..

Advances in genetic testing for cancer predisposing genes -- Diagnosis and management of inheritable pheochromocytomas and paragangliomas -- Diagnosis and management of inheritable kidney cancer syndromes -- Diagnosis and management of inheritable pancreatic cancers/melanomas -- Diagnosis and management of inheritable basal cell skin cancer syndromes -- Diagnosis and management of inheritable adrenal cancers -- Diagnosis and management of inheritable thyroid cancers -- Diagnosis and management of inheritable meningiomas/acoustic neuroma -- Diagnosis and management of inheritable gastric cancer syndromes -- Diagnosis and management of inheritable carcinoid syndromes -- Diagnosis and management of inheritable sarcoma syndromes -- Genetic testing for rare cancer syndromes: the wider issues for patients, families and health professionals.

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.

ISBN: 9783319299983

Standard No.: 10.1007/978-3-319-29998-3doiSubjects--Topical Terms:

336980
Cancer
--Genetic aspects.

LC Class. No.: RC268.4

Dewey Class. No.: 616.994042

Rare hereditary cancers[electronic resource] :diagnosis and management /
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520 $a 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.
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