This lysosomal storage disease is treated by reducing complex sphingolipid accumulation with the glucosylceramide synthase inhibiter miglustat. O Type 1 diabetes Gaucher disease Krabbe disease Fabry disease
This lysosomal storage disease is treated by reducing complex sphingolipid accumulation with the glucosylceramide synthase inhibiter miglustat. O Type 1 diabetes Gaucher disease Krabbe disease Fabry disease
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Q10: What is the correct answer option, pick one of the choices
Transcribed Image Text:This lysosomal storage disease is treated by reducing complex sphingolipid accumulation
with the glucosylceramide synthase inhibiter miglustat.
O Type 1 diabetes
Gaucher disease
Krabbe disease
Fabry disease
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