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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Detalles Bibliográficos
Autores principales: Tanislav, Christian, Feustel, Andreas, Franzen, Wolfgang, Wüsten, Oliver, Schneider, Christian, Reichenberger, Frank, Rolfs, Arndt, Sieweke, Nicole
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039626/
https://www.ncbi.nlm.nih.gov/pubmed/21281467
http://dx.doi.org/10.1186/1471-2261-11-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039626/
https://www.ncbi.nlm.nih.gov/pubmed/21281467
http://dx.doi.org/10.1186/1471-2261-11-6

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