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Article

A family with gastrointestinal amyloidosis associated with variant lysozyme.

Gastroenterology - 1 Oct 2002

Granel Brigitte, Serratrice Jacques, Valleix Sophie, Grateau Gilles, Droz Dominique, Lafon Jacques, Sault Marie-Christine, Chaudier Bernard, Disdier Patrick, Laugier René, Delpech Marc, Weiller Pierre-Jean

Abstract excerpt

Hereditary nonneuropathic systemic lysozyme amyloidosis is a very rare form of amyloidosis, and only 4 families with this condition have been detailed until now in the literature. Clinical manifestations of lysozyme amyloidosis observed until now mainly concerned the kidneys, liver, and digestive tract. We report here a new family with hereditary lysozyme amyloidosis who presented predominantly with...

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PMID: 12360495
DOI: 10.1053/gast.2002.36022

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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