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The Amyloidoses: Clinical Features, Diagnosis and Treatment Cover

The Amyloidoses: Clinical Features, Diagnosis and Treatment

By:  and    
Open Access
|Jul 2012

Abstract

Amyloidosis is a rare disorder in which insoluble amyloid proteins are deposited in body organs, causing abnormal protein build-up in tissues and eventually leading to organ dysfunction and death. It affects less than 200,000 people in the United States, classifying it as a rare disease according to the National Institutes of Health. Definitive determination of the underlying protein is critical since prognosis and treatment of amyloidosis can vary widely depending on the responsible protein. The following paper describes the various types and clinical features of amyloidosis and provides an overview of current diagnostic tools and therapies.

DOI: https://doi.org/10.14797/mdcj-8-3-3 | Journal eISSN: 1947-6108
Language: English
Page range: 3 - 7
Published on: Jul 1, 2012
Published by: Houston Methodist DeBakey Heart & Vascular Center
In partnership with: Paradigm Publishing Services

© 2012 Kelty R. Baker, Lawrence Rice, published by Houston Methodist DeBakey Heart & Vascular Center
This work is licensed under the Creative Commons Attribution-NonCommercial 4.0 License.