Ontology highlight
ABSTRACT: Background
Amyloidosis is defined by abnormal protein folding and subsequent deposition in tissues. Cardiac involvement is usually related to misfolded monoclonal immunoglobulin light chains or misfolded transthyretin; however, apolipoprotein A-1-associated amyloidosis is a hereditary form of amyloidosis resulting from mutations in the AAPOA1 gene that can also result in cardiac amyloidosis. Although there have been advancements in noninvasive algorithms for the diagnosis of cardiac amyloidosis, endomyocardial biopsy (EMB) may still be warranted. All individuals undergoing EMB are susceptible to complications, including tricuspid valve injury resulting in severe tricuspid valve regurgitation.Case summary
Our patient is a 70-year-old white man presented with symptoms of dysp
SUBMITTER: Alomari M
PROVIDER: S-EPMC10733207 | biostudies-literature | 2023 Dec
REPOSITORIES: biostudies-literature