Amyloidosis classification: Difference between revisions
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== Overview == | == Overview == | ||
The more common types of amyloid include AL, AA, Aβ, ATTR and Aβ<sub>2</sub>M from the 15 biologically distinct forms. | |||
==Classification== | ==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: | 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: | ||
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== References == | == References == | ||
{{reflist|2}} | {{reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Disease]] | |||
[[Category:Rheumatology]] | |||
[[Category:Cardiology]] | |||
[[Category:Mature chapter]] | |||
[[Category:Metabolic disorders]] | |||
[[Category:Inborn errors of metabolism]] | |||
[[Category:Endocrinology]] | |||
Revision as of 18:16, 25 October 2012
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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]
Overview
The more common types of amyloid include AL, AA, Aβ, ATTR and Aβ2M from the 15 biologically distinct forms.
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: