9783319894966-331989496X-Polyendocrine Disorders and Endocrine Neoplastic Syndromes (Endocrinology)

Polyendocrine Disorders and Endocrine Neoplastic Syndromes (Endocrinology)

ISBN-13: 9783319894966
ISBN-10: 331989496X
Edition: 2021
Author: Annamaria Colao, Marie-Lise Jaffrain-Rea, Albert Beckers
Publication date: 2021
Publisher: Springer
Format: Hardcover 448 pages
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Book details

ISBN-13: 9783319894966
ISBN-10: 331989496X
Edition: 2021
Author: Annamaria Colao, Marie-Lise Jaffrain-Rea, Albert Beckers
Publication date: 2021
Publisher: Springer
Format: Hardcover 448 pages

Summary

Polyendocrine Disorders and Endocrine Neoplastic Syndromes (Endocrinology) (ISBN-13: 9783319894966 and ISBN-10: 331989496X), written by authors Annamaria Colao, Marie-Lise Jaffrain-Rea, Albert Beckers, was published by Springer in 2021. With an overall rating of 4.5 stars, it's a notable title among other Internal Medicine (Medicine) books. You can easily purchase or rent Polyendocrine Disorders and Endocrine Neoplastic Syndromes (Endocrinology) (Hardcover) from BooksRun, along with many other new and used Internal Medicine books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $0.3.

Description

This comprehensive reference book is meant to support clinicians in the diagnosis and treatment of polyendocrine diseases and endocrine neoplastic syndromes.
Although a large majority of endocrine diseases present as sporadic cases, an increasing proportion can be identified as part of a polyendocrine or systemic syndrome. These include autoimmune endocrine diseases, which may be part of autoimmune polyendocrine disorders (APS) or rare complex disorders such as POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes) or IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked) syndromes. On the other hand, endocrine tumors may develop in a variety of clinical conditions, including multiple endocrine neoplasia (MEN) syndromes, syndromic diseases such as McCune Albright or Carney’s complex, or peculiar familial associations such as pheochromocytoma/paraganglioma syndromes.
The book discusses the significant advances that have been made in the clinical and genetic characterization of such entities, with major implications in terms of diagnosis and clinical management - with special attention to emerging syndromes, familial screening , multidisciplinarity and multimodal treatment. This volume is intended for clinicians, residents, specialists and physicians involved in the diagnosis and treatment of affected patients, including specialists in endocrinology, internal medicine, oncology , genetics and imaging.

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