Familial amyloidosis classification: Difference between revisions
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(Created page with "__NOTOC__ {{Familial amyloidosis}} {{CMG}}; {{AE}} ==Overview== There is no established system for the classification of [disease name]. OR [Disease name] may be classifie...") |
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{{CMG}}; {{AE}} | {{CMG}}; {{AE}} | ||
==Overview== | ==Overview== | ||
Familiar amyloidosis may be classified according to the type of mutant protein into 6 subtypes: Transthyretin amyloidosis (TTR), apolipoprotein AI, cystatin C, lysozyme, fibrinogen A alpha-chain, and apolipoprotein AII. | |||
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==Classification== | ==Classification== | ||
Familiar amyloidosis may be classified according to the type of mutant protein into 6 subtypes: | Familiar amyloidosis may be classified according to the type of mutant protein into 6 subtypes:<ref name="Benson2003">{{cite journal|last1=Benson|first1=Merrill D|title=The hereditary amyloidoses|journal=Best Practice & Research Clinical Rheumatology|volume=17|issue=6|year=2003|pages=909–927|issn=15216942|doi=10.1016/j.berh.2003.09.001}}</ref> | ||
* transthyretin amyloidosis (TTR) | * transthyretin amyloidosis (TTR) | ||
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* cystatin C | * cystatin C | ||
* lysozyme | * lysozyme | ||
* fibrinogen | * fibrinogen A alpha-chain | ||
* apolipoprotein AII | * apolipoprotein AII | ||
Revision as of 23:43, 29 October 2019
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Familial amyloidosis Microchapters |
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Case Studies |
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Familial amyloidosis classification On the Web |
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American Roentgen Ray Society Images of Familial amyloidosis classification |
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Risk calculators and risk factors for Familial amyloidosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Familiar amyloidosis may be classified according to the type of mutant protein into 6 subtypes: Transthyretin amyloidosis (TTR), apolipoprotein AI, cystatin C, lysozyme, fibrinogen A alpha-chain, and apolipoprotein AII.
Classification
Familiar amyloidosis may be classified according to the type of mutant protein into 6 subtypes:[1]
- transthyretin amyloidosis (TTR)
- apolipoprotein AI
- cystatin C
- lysozyme
- fibrinogen A alpha-chain
- apolipoprotein AII
References
- ↑ Benson, Merrill D (2003). "The hereditary amyloidoses". Best Practice & Research Clinical Rheumatology. 17 (6): 909–927. doi:10.1016/j.berh.2003.09.001. ISSN 1521-6942.