Pathogenic mechanisms in Fabry disease
Anderson-Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by deficient activity of the enzyme α-galactosidase A, resulting in progressive accumulation of glycosphingolipids, particularly globotriaosylceramide (Gb3), across multiple organs. FD exhibits marked phenotypic variabi...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
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Frontiers Media S.A.
2026-06-01
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| Schriftenreihe: | Frontiers in Medicine |
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| Online-Zugang: | https://www.frontiersin.org/articles/10.3389/fmed.2026.1867822/full |
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