Rate of progression of transthyretin amyloidosis.

Abstract

Hereditary transthyretin (TTR) amyloidosis is an adult-onset disease characterized mainly by peripheral neuropathy and cardiomyopathy. Although disease progression is usually 5 to 15 years from time of diagnosis to death, no specific measurements of disease progression have been identified. The present study was designed to identify objective parameters to… (More)
DOI: 10.1016/j.amjcard.2011.03.040

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