Fabry Disease: Enzyme Deficiency in the Human Body
Fabry disease is an inherit (genetic or DNA) metabolic fat storage disorder, certain fats (globotriaosylceramide or GL-3) accumulate in the blood vessels over many years, leading to the involvement (or damage) of various tissues and organs of the body, including the heart and kidney. In 1898, two European dermatologists, Johann Fabry of Dortmund, Germany and ...