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Article

Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English family.

QJM : monthly journal of the Association of Physicians - 1 May 2000

Gillmore J D, Booth D R, Rela M, Heaton N D, Rahman V, Stangou A J, Pepys M B, Hawkins P N

Abstract excerpt

A 53-year-old English woman who had been thought to have systemic monoclonal immunoglobulin light chain (AL) amyloidosis was investigated further because of her unusually long 17-year history and a suggestion of renal disease in the family. She was found to have the Glu526Val fibrinogen alpha-chain variant that causes autosomal dominant hereditary systemic amyloidosis. This has not previously been described in a...

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Identifiers

PMID: 10825402
DOI: 10.1093/qjmed/93.5.269

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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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