| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2898611 | Cardiovascular Pathology | 2016 | 4 Pages |
Abstract
Fabry's disease is a lysosomal storage disease characterized by intracellular accumulation of ceramide trihexoside resulting from alpha-galactosidase A deficiency. While the heart is often involved, coronary artery disease and its management in Fabry's disease patients are extremely rare clinical entities. We report a case of a 72-year-old man with left main disease in Fabry's disease with special consideration of the arterial wall pathology.
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Authors
Hiroaki Osada, Naoki Kanemitsu, Masahisa Kyogoku,