Gaucher disease is an inherited disorder caused by the deficiency of the enzyme glucocerebrosidase. This enzyme deficiency leads to the buildup of a fatty substance (glucocerebroside) in cells in the liver, spleen, and bone marrow (Gaucher cells).
The three types of Gaucher disease are described by the presence and severity of nervous system complications.
Gaucher disease is treated with enzyme replacement medicines. Support groups and counseling can be helpful for people with Gaucher disease and for their families. Genetic testing is recommended to identify carriers of the disease and help guide decisions about having children.
Current as of: December 9, 2019
Author: Healthwise Staff
Medical Review:Adam Husney MD - Family Medicine & Patrice Burgess MD - Family Medicine & Martin J. Gabica MD - Family Medicine & Siobhan M. Dolan MD, MPH - Reproductive Genetics
To learn more about Healthwise, visit Healthwise.org.
© 1995-2020 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.