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

Título de la revista
Autores
Martins, A.M.
Ospina, S.
Villalobos, J.
Politei, J.
Varas, C.
Registry Coordinators, Latin America

Fecha
2012-04-01

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Editor
Elsevier

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Resumen
Abstract
Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme ?-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.
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Keywords
Medical and Health Sciences , Pharmacology and Pharmaceutical Sciences
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