Phenyl Ketonuria ( genetic defects in amino-acid metabolism)

Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated, PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. It may also result in a musty smell and lighter skin.

[@charbel424]

Thank you so much for your effort. Wonderfully explained!

[@animatedbiologywitharpan]

Please share my channel link with your friends and help me to reach big audience

[@Doodlemelon3004]

Amazing explaination. Suggest a good elaborate book for genetics please !

[@animatedbiologywitharpan]

I genetics or snustat

[@peteralan1930]

Sir gat b paper solve karwa do

[@Zehra-9809]

Nice explanation

[@animatedbiologywitharpan]

Please share among friends help to reach big audience

[@Zehra-9809]

@@animatedbiologywitharpan ok

[@sabi1808]

Thank u sir

[@animatedbiologywitharpan]

Please share my channel link with your friends and help me to reach big audience

[@vigneshs5286]

First comment