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Persistent increase in cardiac troponin I in Fabry disease: a case report
BACKGROUND: Hypertrophic cardiomyopathy is a frequent manifestation in Fabry disease (FD) - an X-linked lysosomal storage disorder caused by reduced activity of the enzyme α-galactosidase A. In FD an elevation of specific cardiac biomarkers, such as cardiac troponin I (cTNI) has been reported in cas...
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| Main Authors: | , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3039626/ https://ncbi.nlm.nih.gov/pubmed/21281467 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2261-11-6 |
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