Amyloidosis classification: Difference between revisions
Jump to navigation
Jump to search
Megan Merlo (talk | contribs) No edit summary |
|||
Line 7: | Line 7: | ||
==Classification== | ==Classification== | ||
classified according to the respective fibril protein precursor. | |||
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: | ||
{| | {| class="sortable wikitable" | ||
|- | |- | ||
! Official<BR>abb. | ! Official<BR>abb. |
Revision as of 18:53, 7 May 2018
Amyloidosis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Amyloidosis classification On the Web |
American Roentgen Ray Society Images of Amyloidosis classification |
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
classified according to the respective fibril protein precursor.
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: