The amyloidoses: clinical features, diagnosis and treatment.

Kelty R. Baker, Lawrence Rice

Research output: Contribution to journalArticlepeer-review

48 Scopus citations


Amyloidosis is a rare disorder in which insoluble amyloid proteins are deposited in body organs, causing abnormal protein build-up in tissues and eventually leading to organ dysfunction and death. It affects less than 200,000 people in the United States, classifying it as a rare disease according to the National Institutes of Health. Definitive determination of the underlying protein is critical since prognosis and treatment of amyloidosis can vary widely depending on the responsible protein. The following paper describes the various types and clinical features of amyloidosis and provides an overview of current diagnostic tools and therapies.

Original languageEnglish (US)
Pages (from-to)3-7
Number of pages5
JournalMethodist DeBakey cardiovascular journal
Issue number3
StatePublished - 2012

ASJC Scopus subject areas

  • Medicine(all)


Dive into the research topics of 'The amyloidoses: clinical features, diagnosis and treatment.'. Together they form a unique fingerprint.

Cite this