Systemic amyloidosis is a relatively rare multisystem disease caused by the deposition of
misfolded protein in various tissues and organs. It may present to almost any specialty, and …

Amyloidosis is a pathologic and clinical condition resulting from the accumulation of
insoluble aggregates of misfolded proteins in tissues. Extracellular deposition of amyloid …

Cardiac amyloidosis, once considered a rare disease, has garnered significant attention
over the last few years due to three key reasons: first, increased recognition of this disease …

Cardiac amyloidosis describes clinically significant involvement of the heart by amyloid
deposition, which may or may not be associated with involvement of other organs. The …

Cardiac amyloidosis is an under-recognized and potentially fatal cause of heart failure and
other cardiovascular manifestations. It is caused by deposition of misfolded precursor …

The amyloidoses are a group of protein-folding disorders in which≥ 1 organ is infiltrated by
proteinaceous deposits known as amyloid. The deposits are derived from 1 of several …

Cardiac amyloidosis, the primary determinant of prognosis in systemic amyloidoses, is
characterized by infiltration of myocardium by amyloid protein resulting in cardiomyopathy …

Amyloidosis is a severe systemic disease. Cardiac involvement may occur in the three main
types of amyloidosis (acquired monoclonal light-chain, hereditary transthyretin and senile …

Systemic amyloidosis comprises an uncommon group of disorders caused by the
extracellular deposition of misfolded proteins in various organs. Cardiac amyloid deposition …

Amyloidosis is a rare disease in which insoluble extracellular protein fibrils in β-pleated
sheets infiltrate multiple organs, causing organ dysfunction and failure. Amyloidoses are …