Phenylalanine metabolism and Overview of phenylketonuria : Medical Biochemistry : Dr Priyansh jain

[@tnazar9991]

hi sir how are you? in my medical college im fear of studying biochemistry but you made it easy with your great explanation thank you so much sir im your limra student

[@Medvik141]

I am pharmacy students thanks a lot sir "bawaaaaaal"

[@doctorbhanuprakash]

All the best.

[@shehnazmalik8809]

U r amazing sir

[@doctorbhanuprakash]

Thanks a lot

[@intro2123_]

Wonderful

[@khkhmoh4651]

Is it autosomal recessive?
Thank you 🌷

[@DrPriyanshJain]

Auto rece

[@noureenzafar7369]

Thanks u sir

[@jahanvipatel5269]

Sir but maternal enzymes are not working on mom before getting pregnant...then how it will work for...baby?

[@lakshmiprasadyadav4458]

Phenyl ketourea is an autosomal recessive disorder so if the mother is heterozygous ( carrier) then mother will continue to produce enzymes, and in case the husband is diseased or carrier then the foetus may be homozygous and hence diseased but it may not be diagnosed in foetal stage due to mothers hormone crossing olacenta and reaching foetus.
This is what I can think.
I'm a neet aspirant so I'm not sure 😅✌😅

[@jahanvipatel5269]

@@lakshmiprasadyadav4458 tysm sir 💖 it was great explanation actually m preparing for neet exam but I have always faced doubts in genetics...but this video and ur doubt explanation really helped me...alot...😇🙏🏻🌸