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Article

Cutis laxa in hereditary gelsolin amyloidosis.

The British journal of dermatology - 1 Feb 2005

Kiuru-Enari S, Keski-Oja J, Haltia M

Abstract excerpt

BACKGROUND: Hereditary gelsolin amyloidosis (AGel amyloidosis) is an age-associated systemic disease with global distribution, caused by a G654A or G654T gelsolin gene mutation. Cutis laxa is a principal clinical manifestation of this disease. However, only few data on the dermatological involvem...

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Identifiers

PMID: 15727635
DOI: 10.1111/j.1365-2133.2004.06276.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15727635-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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