Cardiac amyloidosis laboratory findings: Difference between revisions

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* [[Brain natriuretic peptide]]
* [[Brain natriuretic peptide]]
* Serum [[transthyretin]]  
* Serum [[transthyretin]]  
* Urinalysis for proteinuria
* Urinalysis for [[proteinuria]]
* Serum and urine electrophoresis
* Serum and urine [[electrophoresis]]
* Serum electrolytes
* Serum [[electrolytes]]


==References==
==References==

Revision as of 16:47, 4 May 2013

Cardiac amyloidosis Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]; Aarti Narayan, M.B.B.S [3]; Lakshmi Gopalakrishnan, M.B.B.S. [4]

Overview

There is no specific diagnostic blood test, radiograph, or scan that can be used to diagnose amyloidosis; hence, awareness of the disease is necessary to identify patients with amyloidosis.[1]

Laboratory Findings

The following are the laboratory tests included in the management of cardiac amyloidosis:

References

  1. Hawkins PN (1997). "The diagnosis, natural history and treatment of amyloidosis. The Goulstonian Lecture 1995". Journal of the Royal College of Physicians of London. 31 (5): 552–60. PMID 9429195. |access-date= requires |url= (help)


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