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Article

Early cardiovascular remodelling in Fabry disease.

Journal of inherited metabolic disease - 1 Jan 2014

Costanzo Luca, Buccheri Sergio, Capranzano Piera, Di Pino Luigi, Curatolo Giuseppina, Rodolico Margherita, Leggio Stefano, Blundo Anita, Tamburino Corrado, Monte Ines

Abstract excerpt

AIMS: Fabry disease (FD) is a rare X-linked genetic disorder caused by the deficiency or absent activity of lysosomal α-galactosidase A. Cardiovascular remodelling is a hallmark of FD. The present study aimed to comprehensively evaluate the cardiac, vascular and microvascular status in a population of patients with genetic mutations for FD without left ventricular hypertrophy (LVH). METHODS AND RESULTS: This...

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Source

Identifiers

PMID: 23615762
DOI: 10.1007/s10545-013-9607-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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