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
- ↑ 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
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