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Meet Taran – a young boy living with a rare, genetic disorder known as acid sphingomyelinase deficiency, or #ASMD. Taran is part of our Rare Humanitarian Program, which lends a helping hand to eligible patients all over the world affected by certain rare diseases. Our program aims to facilitate access to suitable health care for eligible patients who need it. At Sanofi, we remain committed to pursuing better care for rare. Join us in recognizing the pursuit of equity in the care and treatment of
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Which of the following enzymes is most likely deficient in this patient?
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