Hereditary Transthyretin Amyloidosis: A Comprehensive Guide to Diagnosis and Treatment

By Claudia Sommer, Frank Birklein, and Ernst Hund, leading experts in the field of amyloidosis research, this book provides an in-depth exploration of hereditary transthyretin amyloidosis, a complex and rare genetic disorder that affects various regions worldwide, including Portugal, Sweden, and Japan.

This debilitating condition is characterized by the manifestation of amyloid neuropathy, posing significant diagnostic challenges due to its variable clinical presentation. The timely and accurate diagnosis of hereditary transthyretin amyloidosis is crucial, as it enables the deployment of novel therapeutic approaches that can positively impact the disease’s progression.

The authors have meticulously compiled the current state of knowledge on hereditary transthyretin amyloidosis in this comprehensive guide, covering the clinical, pathological, and genetic aspects of diagnosis, organ manifestations, and current and potential future treatments.

This book is an invaluable resource for healthcare professionals, researchers, and patients seeking to understand the complexities of this rare disease and stay abreast of the latest advancements in its diagnosis and management.

Book Details:

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