Cardiac amyloidosis classification
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sabawoon Mirwais, M.B.B.S, M.D.[2]
Overview
Cardiac amyloidosis can be classified based on the type of amyloid that infiltrates the heart. The types of amyloid that commonly deposit in the heart are immunoglobulin light chain (AL) and transthyretin (ATTR). These two types of amyloid can result in cardiac AL amyloidosis and cardiac transthyretin amyloidosis.
Classification
- Cardiac amyloidosis can be classified based on the type of amyloid that infiltrates the heart.[1]
- The types of amyloid that commonly deposit in the heart are:
- Immunoglobulin light chain (AL)
- Transthyretin (ATTR)
References
- ↑ Martinez-Naharro A, Hawkins PN, Fontana M (April 2018). "Cardiac amyloidosis". Clin Med (Lond). 18 (Suppl 2): s30–s35. doi:10.7861/clinmedicine.18-2-s30. PMC 6334035. PMID 29700090.