Alpha-Galactosidase A Levels in Colombian Males with End-Stage Renal Disease: Ten Years of Selective Screening in Dried Blood Spots

Abstract Fabry disease is a metabolic alteration linked to an enzymatic deficiency of Alpha-Galactosidase A, this disorder compromises the sphingolipid metabolism, leading to an accumulation of Mens Skirts lysosomal globotriaosylceramide and is inherited in an X-linked recessive way.The diagnostic of this disease, in general, requires the confirmat

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