Fabry disease: the importance of the enzyme replacement therapy (TRE), treating quickly and efficiently
Fabry Disease is a lysosomal disorder due to the absence or deficiency of the Alpha galactosidase A enzyme that causes a pathological accumulation of glycosphingolipids mainly in the endothelial cells, vascular smooth muscle cells and podocytes among others. Enzyme replacement therapy is the only op...
Main Authors: | , , , , , |
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Format: | Article |
Language: | Spanish |
Published: |
Asociación Regional de Diálisis y Trasplantes Renales de Capital Federal y Provincia de Buenos Aires
2014-06-01
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Series: | Revista de Nefrología, Diálisis y Trasplante |
Subjects: | |
Online Access: | http://www.revistarenal.org.ar/index.php/rndt/article/view/108 |