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Article

Fabry disease in patients with hypertrophic cardiomyopathy (HCM).

Zeitschrift fur Kardiologie - 1 Dec 2002

Beer G, Reinecke P, Gabbert H E, Hort W, Kuhn H

Abstract excerpt

Fabry disease is an X-linked recessive lysosomal storage disorder with variable phenotype characterized by the accumulation of glycosphingolipid in various tissues. Unlike patients with the classical systemic Fabry disease entity, who present with multiple organ involvement, patients with a cardiac variant of Fabry disease are characterized mainly by myocardial hypertrophy. Therefore, the cardiac variant of Fabry...

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Identifiers

PMID: 12490989
DOI: 10.1007/s00392-002-0870-7

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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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