Phenylketonuria (PKU) || Phenylalanine Metabolism

Phenylketonuria - This video is on Phenylketonuria with NEET PG and AIIMS MCQS.
Phenylketonuria is an inborn error of phenylalanine metabolism, associated with the inability to convert phenylalanine to tyrosine because deficiency of Phenylalanine Hydoxylase enzyme.
Phenylketonuria is inherited as Autosomal recessive manner
It result in accumulation of phenylalanine in tissues and blood and its increased excretion in urine.

[@kanishjain9390]

So helpful video and much needed. Thank you. You can also checkout my article in pediatriconcall.com on the same topic

[@Biochemistrybasics]

Will surely check. Thanks for the sharing 😇

[@errdftyy]

Best lecture sir thanks

[@Biochemistrybasics]

Thank you sir. Please spread the word and Tk cr 😇

[@sudhu4ever]

Use thumbnails and logo to ur channel...

[@عامرحسين-و7ح]

Explanation is so great but i have question is dopamine differentiatate between type 1and type 2 how happen can answer meeeeeee plssssd

[@Biochemistrybasics]

Sorry did not understand the question. Can you brief it again

[@عامرحسين-و7ح]

@@Biochemistrybasics is dopamine has diagnostic role in types of phenylketonuria

[@Biochemistrybasics]

@@عامرحسين-و7ح not exactly in the diagnosis

[@gulfwarveteran8528]

Covered everything in detail thanx sir

[@farheensaba17]

Wonderfully explained...!
Thank you sir

[@Biochemistrybasics]

My pleasure Farheen. Please spare a few minutes and do spread the word about the channel among your batchmates and friends

[@anshparabtani1536]

thanks sir ...it helped a lot ......ansh here.

[@Biochemistrybasics]

Hey ansh. My pleasure 😊

[@prashanthegde6461]

Explained in very simple and effective way

[@Biochemistrybasics]

Thanks prashant. Keep loving biochemistry 😊

[@233vasudhayadav2]

Simple and very helpful

[@Biochemistrybasics]

Thanks 😊