Fabry Disease: Symptoms, Causes, Treatment

The Fabry disease is an inherited condition that is associated with an accumulation of a particular type of lipid in different  body structures (Genetics Home Reference, 2016). This medical condition has a genetic origin associated with the X chromosome and its clinical characteristics are caused by the presence of deficient levels  of the α-galactosidase enzyme (Martínez-Mechón et al., 2004). The clinical … Read more