When should cardiologists suspect Anderson-Fabry disease?

Abstract

Anderson-Fabry disease is a lysosomal storage disorder caused by α-galactosidase defects and progressive intracellular accumulation of globotriaosylceramide. The disease can be specifically treated with enzyme replacement therapy. Hemizygous men and heterozygous women can develop cardiac disease. Whereas men experience the most severe clinical phenotype… (More)
DOI: 10.1016/j.amjcard.2010.07.016

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