What is Niemann-Pick Type A?
Niemann-Pick disease type A is an inherited condition that occurs in early infancy; it is characterized as a deficiency of the acid sphingomyelinase enzyme, which normally breaks down a fatty substance called sphingomyelin. The accumulation of sphingomyelin primarily occurs in the liver and spleen.
How do members experience Niemann-Pick Type A?
Top 5 symptoms reported by people with Niemann-Pick Type A*
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Top treatments taken by people for Niemann-Pick Type A*
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Who has Niemann-Pick Type A on PatientsLikeMe?
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Talk to people with Niemann-Pick Type A
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