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Cardiac magnetic resonance imaging illustrating Anderson–Fabry disease progression
Anderson–Fabry disease is an X-linked lysosomal storage disorder resulting from a deficiency of the enzyme α-galactosidase A (α-Gal A) and subsequent cellular storage of the enzyme's substrate globotriaosylceramide (Gb3) and related glycosphingolipids. We report a case of Anderson–Fabry disease...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The British Institute of Radiology.
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3473621/ https://ncbi.nlm.nih.gov/pubmed/21088081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1259/bjr/52065763 |
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