Clinical and pathologic characteristics of hereditary apolipoprotein A ‐ I amyloidosis in I reland

This is an interesting case series which described the clinical features of hereditary amyloidosis due to apolipoprotein A‐I deficiency. It will improve the awareness of this rare kind of hereditary amyloidosis.

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Bibliographic Details
Published in:Nephrology (Carlton, Vic.) Vic.), 2013-08, Vol.18 (8), p.549-554
Main Authors: Traynor, Carol A, Tighe, Donal, O'Brien, Frank J, Leavey, Sean F, Dorman, Anthony M, Denton, Mark D, Magee, Colm, Conlon, Peter J
Format: Article
Language:English
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Description
Summary:This is an interesting case series which described the clinical features of hereditary amyloidosis due to apolipoprotein A‐I deficiency. It will improve the awareness of this rare kind of hereditary amyloidosis.
ISSN:1320-5358
1440-1797
DOI:10.1111/nep.12108