[Comparison of patients from a Spanish Registry of Fabry disease in two periods].

Abstract excerpt

BACKGROUND AND OBJECTIVE: Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by a deficiency of the enzyme alpha-galactosidase A, that leads to multiorgan dysfunction and premature death. Data from the first 24 Spanish patients enrolled on the Fabry Outcome Survey (FOS) were published in 2004, with a significant increase in the number of patients since then. This manuscript analyzes whether...

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