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Clinical and pathologic characteristics of hereditary apolipoprotein A-I amyloidosis in Ireland.

Nephrology (Carlton, Vic.) - 1 Aug 2013

Traynor Carol A, Tighe Donal, O'Brien Frank J, Leavey Sean F, Dorman Anthony M, Denton Mark D, Magee Colm, Conlon Peter J

Abstract excerpt

AIM: Apolipoprotein A-I amyloidosis is a rare, autosomal dominant disorder characterized by progressive accumulation of amyloid fibrils in tissues, leading to renal and hepatic disease. We describe the clinical manifestations and pathologic features of kidney disease in three Irish families. METHODS: This observational study examines all known cases of chronic kidney disease due to hereditary apolipoprotein A-I...

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PMID: 23730806
DOI: 10.1111/nep.12108

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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