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Article

Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation.

Journal of internal medicine - 1 Jul 2012

Sattianayagam P T, Gibbs S D J, Rowczenio D, Pinney J H, Wechalekar A D, Gilbertson J A, Hawkins P N, Lachmann H J, Gillmore J D

Abstract excerpt

OBJECTIVES: Lysozyme amyloidosis (ALys) is a form of hereditary systemic non-neuropathic amyloidosis, which is inherited in an autosomal dominant fashion. Lysozyme, which is the amyloidogenic precursor protein in ALys, is a ubiquitous bacteriolytic enzyme synthesized by hepatocytes, polymorphs and macrophages. The aim of this study is to describe the phenotype and outcome of patients with ALys including the role...

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Identifiers

PMID: 21988333
DOI: 10.1111/j.1365-2796.2011.02470.x

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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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