Lysosomal Storage Disorders: Sphingolipidoses - CRASH! Medical Review Series

[@DrSAlex25]

I wonder why this channel doesn’t have more subscribers … amazing!! Easy to understand and quick to the point ❤ thank you so much

[@hishamsallam7324]

thank you so much for such an amazing talent in explaining

[@Kartik-ij2vy]

You made this topic easy ,thanks

[@woloabel]

We have here Five Autosomal Recessive Diseases of Lysosomal Storage Disorders (Pathology of Metabolism and Degeneration Types) and one particular to Pediatric Males: 1) Tay-Sachs Disease, 2) Niemann Pick, 3) Krabbe, 4)Fabry's Disease (XLR), 5) Gauchers Disease and 6) Metachromatic Lipodystrophy and they all have their respective Enzyme Deficiency, namely and respectively Hexoaminidase (Ganglioside Buildup), Sphingomyelinase (Sphingomyelin), Galactocerebrosidase (Galactocerebroside), Alpha Galactosidase (Ceramide Trihexoside) and Arylsulfatase A (Sulfatides)....Give me a point now. MD Paul Bolin, du bist ausgezeichnet!

[@ФилипАтакер]

thank you so much for this! it is greatly appreciated

[@ntandachikweti2090]

Insightful Thanks

[@lord-mf2sf]

Thank you sir❤️❤️❤️

[@zarakafridi2355]

Thank you sir may Allah bless you