Fabry Disease and the Hope of Enzyme Replacement Therapy
Fabry disease is a rare, X-linked genetic disorder that affects the way the body breaks down a specific type of fat, called globotriaosylceramide (Gb3). Gb3 can build up in cells throughout the body, including the heart, kidneys, skin, and nervous system. This buildup can lead to a variety of health problems, including heart failure, kidney…
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