P12—Fabry Disease in Latin America: A Report From the Fabry Registry

Introduction Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme α-galactosidase A. The Fabry Registry is a global, observational, and voluntary program designed to collect clinical data related to the onset, progression, and treatment of Fabry...

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Bibliographic Details
Published in:Clinical therapeutics Vol. 34; no. 4; p. e23
Main Authors: Martins, A.M, Ospina, S, Villalobos, J, Politei, J, Varas, C
Format: Journal Article
Language:English
Published: Bridgewater EM Inc USA 01-04-2012
Elsevier Limited
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Summary:Introduction Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme α-galactosidase A. The Fabry Registry is a global, observational, and voluntary program designed to collect clinical data related to the onset, progression, and treatment of Fabry disease.
ISSN:0149-2918
1879-114X
DOI:10.1016/j.clinthera.2012.03.042