Niemann Pick Disease
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- Опубліковано 6 вер 2024
- 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.
Thanks for the simplified explanation 👍
Could you make a deep explanatory video about all types of vasculitis, please?
Thank you in advance!
Surely I will
Treatment ??
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