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Pathological findings in a patient with Fabry disease who died after 2.5 years of enzyme replacement
We describe the postmortem findings of a 47-year-old man with Fabry disease, an X-linked glycolipid storage disorder, who was on enzyme replacement therapy with recombinant α-galactosidase A for more than 2 years. The patient had widespread atherosclerotic coronary artery disease that culminated in...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2005
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2288734/ https://ncbi.nlm.nih.gov/pubmed/16315019 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00428-005-0089-x |
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