"Dear Doctor's Participate In This Fun And Exciting Quiz On Fabry Disease, named after the German physician Johann Fabry, is a rare and progressive genetic disorder that falls under the category of lysosomal storage diseases. This condition primarily affects the metabolism of lipids due to an inherited deficiency or malfunctioning of an enzyme called alpha-galactosidase A (a-Gal A). The absence or dysfunction of this crucial enzyme leads to a harmful buildup of globotriaosylceramide (GL-3) in various tissues and organs throughout the body. Consequently, individuals with Fabry Disease experience a wide range of symptoms that can manifest differently from person to person. Participate Now "
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