Hereditäre Amyloidneuropathien (UNI-MED Science) (German Edition), 2nd Edition

By Claudia Sommer, Frank Birklein, Ernst Hund
Hereditäre Transthyretin-Amyloidosen mit der Hauptmanifestation der Amyloidneuropathie sind nicht nur in Endemieländern wie Portugal, Schweden und Japan, sondern gerade auch in Regionen, wo diese Erkrankungen sporadisch und selten vorkommen, ein relevantes klinisches Problem. Das zwischen den Unterformen variable klinische Bild stellt die Diagnostik vor eine Herausforderung. Neue Therapiemöglichkeiten eröffnen Chancen und erfordern eine frühzeitige korrekte Diagnose. Die Erkrankung ist noch nicht heilbar, aber der ansonsten unaufhaltsam progrediente Krankheitsverlauf lässt sich positiv beeinflussen.Die Autoren dieses Buches haben in der 2. Auflage den aktuellen Stand des Wissens zu den hereditären Transthyretin-Amyloidosen interdisziplinär zusammengefasst, wobei die klinische, pathologische und genetische Diagnostik ebenso beschrieben wird wie Organmanifestationen sowie aktuelle und potenzielle zukünftige Therapien.

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The hereditary transthyretin amyloidosis is a rare genetic disease that affects the body’s ability to produce the protein that transports thyroid hormone and vitamin A. This disease can cause several health problems, including nerve damage, heart disease, and kidney damage. In recent years, new therapies have emerged that may help slow down the progression of the disease, giving hope to affected individuals and their families.

In their book, Claudia Sommer, Frank Birklein, and Ernst Hund provide an interdisciplinary overview of the current state of knowledge of hereditary transthyretin amyloidosis. This 2nd edition covers clinical, pathological, and genetic diagnostics, as well as organ manifestations and current and potential future therapies. The book is written in German.

One of the most significant challenges in diagnosing hereditary transthyretin amyloidosis is the variability of clinical symptoms between different subtypes. Because the disease is rare, it’s often misdiagnosed, leading to delays in treatment and management. This book aims to provide physicians and other healthcare professionals with a comprehensive reference that can help them diagnose and treat this debilitating disease.

The authors’ inter-disciplinary approach to the topic is a significant strength of the book. They combine clinical observations with knowledge of genetics to give readers a well-rounded understanding of the disease. The authors also provide detailed information on the latest therapeutic approaches, including gene therapy, which shows potential for the treatment of hereditary transthyretin amyloidosis.

For individuals affected by hereditary transthyretin amyloidosis, this book offers hope and guidance. It provides a comprehensive roadmap of the disease and its treatment, which can help them manage their condition proactively.

Overall, I highly recommend this book to anyone interested in hereditary transthyretin amyloidosis. The authors’ in-depth knowledge of the disease has allowed them to produce an authoritative and up-to-date reference resource. This book can help healthcare professionals diagnose and treat this rare disease more effectively and provide affected individuals with hope and a sense of control over their condition.

If you or someone you know has been affected by hereditary transthyretin amyloidosis, I urge you to order a copy of this book today. Its informative and comprehensive content can provide valuable guidance and support in managing this debilitating disease.

Product Details

• ASIN ‏ : ‎ B098R5NCMV
• Publisher ‏ : ‎ UNI-MED Verlag AG; 2nd edition
• Language ‏ : ‎ German
• ISBN-10 ‏ : ‎ 3837424030
• ISBN-13 ‏ : ‎ 978-3837424034