Niemann–Pick disease (/ n iː m ən ˈ p ɪ k / nee-mən-PIK)  is a group of inherited severe metabolic disorders that allows a certain kind of fat to accumulate ...
Niemann-Pick disease is a condition that affects many body systems. It has a wide range of symptoms that vary in severity. Niemann-Pick disease is divided ...
The National Niemann-Pick Disease Foundation supports and promotes research to find treatments and a cure for all types of Niemann-Pick Disease, and we provide ...
Niemann–Pick type C is a lysosomal storage disease associated with mutations in NPC1 and NPC2 genes. Niemann–Pick type C affects an estimated 1:150,000 people. 
PubMed Health includes over 36,000 systematic reviews, often with consumer summaries to explain their results. Systematic reviews find answers to the question "What ...
There is no cure or effective treatment for Niemann-Pick. Mayo specialists work as a team to help people manage the debilitating symptoms of the disease.
Niemann-Pick Disease is one of a group of lysosomal storage diseases that affect metabolism and that are caused by genetic mutations. The three most commonly ...
Niemann-Pick disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
Niemann-Pick disease is a group of diseases passed down through families (inherited) in which fatty substances called lipids collect in the cells of the ...
Clinical characteristics. Niemann-Pick disease type C (NPC) is a lipid storage disease that can present in infants, children, or adults. Neonates can present with ...