Niemann-Pick disease is a rare genetic disorder that renders the body incapable of transporting cholesterol and other lipids inside of cells. The result is a build-up of these fatty substances in various areas of the body, including the brain.
There are four variations of Niemann-Pick disease, each with their own symptoms, onset, and life expectancy. Sadly, Nieman-Pick disease is often fatal. Treatment centers around managing the condition, and extending life expectancy. There is presently no cure.
Keep reading to learn more about Niemann-Pick disease, including the causes, diagnosis, and outlook for the condition.
What is Niemann-Pick disease?
Those with Niemann-Pick may be categorized into A, B, C (NPC1 or NPC2), or E variations of the disease, all of which manifest differently with unique symptoms. While Type A and B sufferers tend to develop symptoms early in life, those with Type C may be afflicted at any time if their genetic make-up is conducive to the disease. Type E suff