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- Publisher
- de Gruyter
- Copyright
- © 2018 Polish Society of Hematology and Transfusion Medicine, Insitute of Hematology and Transfusion Medicine, Published by Sciendo
- eISSN
- 2300-7117
- DOI
- 10.2478/ahp-2018-0002
- Publisher site
- See Article on Publisher Site
Abstract
AbstractCardiac amyloidosis is a rare and often-misdiagnosed disorder. Among other forms of deposits affecting the heart, immunoglobulin-derived light-chain amyloidosis (AL amyloidosis) is the most serious form of the disease. Delay in diagnosis and treatment may have a major impact on the prognosis and outcomes of patients. This review focuses on the presentation of the disorder and current novel approaches to the diagnosis of cardiac involvement in AL amyloidosis.
Journal
Acta Haematologica Polonica – de Gruyter
Published: Mar 30, 2018
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