Cardiac amyloidosis causes: Difference between revisions
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==Overview== | ==Overview== | ||
The causes of cardiac amyloidosis vary based on the cause of the [[systemic]] [[amyloidosis]]. | |||
==Causes== | ==Causes== | ||
*The | *The causes of cardiac [[amyloidosis]] vary based on the cause of the [[systemic]] [[amyloidosis]]. | ||
*Enlisted below are the types of the systemic amyloidosis that are more likely to involve the heart: | *Enlisted below are the types of the systemic amyloidosis that are more likely to involve the [[heart]]: | ||
:*[[Primary amyloidosis]]<ref name="pmid9302305">{{cite journal |author=Falk RH, Comenzo RL, Skinner M |title=The systemic amyloidoses |journal=[[The New England Journal of Medicine]] |volume=337 |issue=13 |pages=898–909 |year=1997 |month=September |pmid=9302305 |doi=10.1056/NEJM199709253371306 |url=http://www.nejm.org/doi/abs/10.1056/NEJM199709253371306?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed |accessdate=2012-02-13}}</ref><ref name="pmid10319082">{{cite journal |author=Gertz MA, Lacy MQ, Dispenzieri A |title=Amyloidosis: recognition, confirmation, prognosis, and therapy |journal=[[Mayo Clinic Proceedings. Mayo Clinic]] |volume=74 |issue=5 |pages=490–4 |year=1999 |month=May |pmid=10319082 |doi=10.4065/74.5.490 |url=http://linkinghub.elsevier.com/retrieve/pii/S0025-6196(11)65130-6 |accessdate=2012-02-13}}</ref> | :*[[Primary amyloidosis]]<ref name="pmid9302305">{{cite journal |author=Falk RH, Comenzo RL, Skinner M |title=The systemic amyloidoses |journal=[[The New England Journal of Medicine]] |volume=337 |issue=13 |pages=898–909 |year=1997 |month=September |pmid=9302305 |doi=10.1056/NEJM199709253371306 |url=http://www.nejm.org/doi/abs/10.1056/NEJM199709253371306?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed |accessdate=2012-02-13}}</ref><ref name="pmid10319082">{{cite journal |author=Gertz MA, Lacy MQ, Dispenzieri A |title=Amyloidosis: recognition, confirmation, prognosis, and therapy |journal=[[Mayo Clinic Proceedings. Mayo Clinic]] |volume=74 |issue=5 |pages=490–4 |year=1999 |month=May |pmid=10319082 |doi=10.4065/74.5.490 |url=http://linkinghub.elsevier.com/retrieve/pii/S0025-6196(11)65130-6 |accessdate=2012-02-13}}</ref> | ||
:*[[Familial amyloidosis|Familial or hereditary transthyretin (TTR)-related form]] | :*[[Familial amyloidosis|Familial or hereditary transthyretin (TTR)-related form]] | ||
Latest revision as of 21:21, 30 October 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sabawoon Mirwais, M.B.B.S, M.D.[2]
Overview
The causes of cardiac amyloidosis vary based on the cause of the systemic amyloidosis.
Causes
- The causes of cardiac amyloidosis vary based on the cause of the systemic amyloidosis.
- Enlisted below are the types of the systemic amyloidosis that are more likely to involve the heart:
References
- ↑ Falk RH, Comenzo RL, Skinner M (1997). "The systemic amyloidoses". The New England Journal of Medicine. 337 (13): 898–909. doi:10.1056/NEJM199709253371306. PMID 9302305. Retrieved 2012-02-13. Unknown parameter
|month=ignored (help) - ↑ Gertz MA, Lacy MQ, Dispenzieri A (1999). "Amyloidosis: recognition, confirmation, prognosis, and therapy". Mayo Clinic Proceedings. Mayo Clinic. 74 (5): 490–4. doi:10.4065/74.5.490. PMID 10319082. Retrieved 2012-02-13. Unknown parameter
|month=ignored (help)