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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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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

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