Amyloidosis classification

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Classification • Primary amyloidosis • Secondary amyloidosis • Familial amyloidosis • Wild-type (senile) amyloidosis • Cardiac amyloidosis • Beta-2 microglobulin related amyloidosis • Gelsolin related amyloidosis • Lysozyme amyloid related amyloidosis • Leucocyte cell-derived chemotaxin 2 related amyloidosis • Fibrinogen A alpha-chain associated amyloidosis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]

Classification

Amyloidosis may be classified according to precursor amyloidogenic protein into different subtypes, include:

Name	Amyloidogenic protein	Clinical syndrome
AL	Monoclonal gammopathy	Light chains of immunoglobulines
AA	Serum amyloid A protein	Chronic inflammation related amyloidosis
AF	Mutant transthyretin, A1-apolipoprotein, gelsolin, fibrinogen, lysozyme, etc.	Familial polyneuropathy/cardiomyopathy/nephropathy
ATTRwt	Transthyretin-related amyloidosis, wild-type	Senile restrictive cardiomyopathy
AH	ß2-microglobulin	Dialysis-related amyloidosis