Wild-type (senile) amyloidosis history and symptoms

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

History and Symptoms

History

  • The clinical features of wild-type (senile) amyloidosis depend on the type of organ or organ system involved.
  • Wild-type (senile) amyloidosis, classified as systemic amyloidosis, can involve any organ in the body.
  • Cardiac and peripheral nerves involvement can result in clinically evident pathology.[1]
  • The most commonly involved organ is the heart and majority of the patients present with signs and symptoms of heart failure.

Common Symptoms

Less Common Symptoms

References

  1. Ilia G. Halatchev, Jingsheng Zheng & Jiafu Ou (2018). "Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA), previously known as senile cardiac amyloidosis: clinical presentation, diagnosis, management and emerging therapies". Journal of thoracic disease. 10 (3): 2034–2045. doi:10.21037/jtd.2018.03.134. PMID 29707360. Unknown parameter |month= ignored (help)