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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...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Espanhol |
| Publicado em: |
Asociación Regional de Diálisis y Trasplantes Renales de Capital Federal y Provincia de Buenos Aires
2014-06-01
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| Colecção: | Revista de Nefrología, Diálisis y Trasplante |
| Assuntos: | |
| Acesso em linha: | http://www.revistarenal.org.ar/index.php/rndt/article/view/108 |
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