Amyloidosis classification: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Amyloidosis}} | {{Amyloidosis}} | ||
{{CMG}} | {{CMG}}; {{AE}} | ||
== Overview == | == Overview == | ||
Of the 15 biologically distinct forms of amyloid, the most common ones include AL, AA, Aβ, ATTR and Aβ<sub>2</sub>M. | Of the 15 biologically distinct forms of amyloid, the most common ones include AL, AA, Aβ, ATTR and Aβ<sub>2</sub>M. | ||
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== References == | == References == | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Rheumatology]] | [[Category:Rheumatology]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Endocrinology]] | [[Category:Endocrinology]] | ||
{{WH}} | |||
{{WS}} | |||
Revision as of 16:51, 20 July 2016
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Amyloidosis Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Amyloidosis classification On the Web |
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American Roentgen Ray Society Images of Amyloidosis classification |
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Risk calculators and risk factors for Amyloidosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Of the 15 biologically distinct forms of amyloid, the most common ones include AL, AA, Aβ, ATTR and Aβ2M.
Classification
There are 15 biologically distinct forms of amyloid, some more clinically significant than others. Following is a brief description of the more common types of amyloid: