Anderson-Fabry disease: Ten-year outcome of enzyme replacement therapy in a renaltransplant patient
Anderson-Fabry disease (AFd) is a rare disorder characterised by the deficiency or absence of lysosomal enzymatic alpha-galactosidase A activity (α-Gal A) that leads to progressive and systemic accumulation of glycosphingolipids. The clinical manifestations are variable but kidney disease usually ma...
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| Other Authors: | , |
| Format: | article |
| Language: | eng |
| Published: |
2016
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| Online Access: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692016000200007 |
| Country: | Portugal |
| Oai: | oai:scielo:S0872-01692016000200007 |