Skip to Content
Niemann-Pick disease is a rare inherited degenerative nerve
disease caused by the deficiency of the enzyme called sphingomyelinase, which
leads to the buildup of a fatty substance (sphingomyelin) in cells in the
liver, spleen, lymph nodes, and bone marrow. Niemann-Pick disease is most
commonly seen in families of Eastern European (Ashkenazi) Jewish
At least five types of Niemann-Pick disease have been
identified. The most common are type A and type B.
There is no treatment for Niemann-Pick disease. Support
groups and counseling can be helpful for people with Niemann-Pick 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:
February 20, 2015
Patrice Burgess, MD - Family Medicine & Siobhan M. Dolan, MD, MPH - Reproductive Genetics
How this information was developed to help you make better health decisions.
To learn more, visit Healthwise.org
© 1995-2015 Healthwise, Incorporated. Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.
© Copyright 2015 Rush-Copley Medical Center • 2000 Ogden Avenue; Aurora, IL 60504
Main: 630-978-6200 • Physician Referral & Information: 630-978-6700 or 866-4COPLEY (866-426-7539)