Overview
- Enhances our understanding of the genetic basis of endocrine diseases
- Covers both the molecular and clinical consequences of genetic alterations
- Highlights the most common human endocrine diseases and syndromes
Part of the book series: Experientia Supplementum (EXS, volume 111)
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Table of contents (20 chapters)
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Front Matter
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Endocrine Diseases Inherited as Monogenic Traits: Hormone Resistance Syndromes
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Front Matter
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Endocrine Diseases Inherited as Monogenic Traits: Hereditary Diseases Predisposing to Endocrine Tumors
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Front Matter
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Endocrine Diseases Inherited as Monogenic Traits: Monogenic Diseases Predisposing to Hormone Deficiency, Infertility and Diabetes Mellitus
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Front Matter
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Keywords
About this book
This book provides a comprehensive overview of the genetic basis underlying endocrine diseases. It covers both the molecular and clinical consequences of these genetic defects, as well as the relevance for clinical care, highlighting issues of genetic counseling.
Several endocrine diseases have a genetic background, and contemporary research in the field plays a crucial role in the clinical care of endocrine diseases. In recent years, there have been major developments in our understanding of the genetic basis of endocrine diseases. Several novel genes and mutations predisposing individuals to monogenic endocrine diseases have been discovered, and with the advent of next generation sequencing, a huge amount of new data has become available. Further, novel molecular mechanisms, such as genomic imprinting, have been implicated in the pathogenesis of endocrine diseases.
A better understanding of the genetic background of these diseases is relevant not only from the research perspective, but also in terms of clinical care. As such, this book is an essential read for both researchers and clinicians working in the field.
Editors and Affiliations
About the editors
Peter Igaz MD MSc PhD DSc is full professor of medicine and head of the 2nd Department of Internal Medicine at Semmelweis University Budapest. He has boarding exams in internal medicine, endocrinology and clinical genetics. His research interests include adrenal tumors, multiple endocrine neoplasia syndromes and neuroendocrine tumors focusing both on classical genetics, microRNAs and other non-coding RNA molecules. He has published over 140 scientific papers.
Attila Patocs MD MSc PhD DSc is associate professor of molecular genetics and laboratory medicine at the Department of Laboratory Medicine of Semmelweis University, and also the head of molecular genetics laboratory at the National Institute of Oncology in Budapest. He has boarding exams in laboratory medicine and molecular genetic diagnostics. His research is focused on hereditary cancer syndromes, endocrine tumors and biomarkers. He has published over 180 scientific papers.
Bibliographic Information
Book Title: Genetics of Endocrine Diseases and Syndromes
Editors: Peter Igaz, Attila Patócs
Series Title: Experientia Supplementum
DOI: https://doi.org/10.1007/978-3-030-25905-1
Publisher: Springer Cham
eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)
Copyright Information: Springer Nature Switzerland AG 2019
Hardcover ISBN: 978-3-030-25904-4Published: 17 October 2019
Softcover ISBN: 978-3-030-25907-5Published: 17 October 2020
eBook ISBN: 978-3-030-25905-1Published: 06 October 2019
Series ISSN: 1664-431X
Series E-ISSN: 2504-3692
Edition Number: 1
Number of Pages: XIX, 473
Number of Illustrations: 21 b/w illustrations, 51 illustrations in colour
Topics: Molecular Medicine, Human Genetics
Industry Sectors: Biotechnology, Chemical Manufacturing, Consumer Packaged Goods, Health & Hospitals, Pharma