Niemann Pick Disease

Niemann-Pick disease A and B are characterized by lysosomal accumulation of sphingomyelin due to an inherited deficiency of sphingomyelinase.
Niemann-Pick disease type C (NPC) is due to mutation in NPC 1 and 2 gene.

[@anuragsharma0003]

Thanks for the simplified explanation 👍

[@Krisler12]

Could you make a deep explanatory video about all types of vasculitis, please?
Thank you in advance!

[@pathologysimplified]

Surely I will

[@user-xe1nn7ys1c]

Treatment ??

[@asifhussain2555]

Hello mam , my two kids diagnosed with NPC , one kid 1 yr old and one is 3 yrs old , pls suggest what to do . Doctor is suggesting lever transplant