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0:35
YouTube
Paediatrics Simplified
Don't Ignore These PHENYLKETONURIA Warning Signs || phenylalanine || PKU || amino acid metabolism
Phenylketonuria (PKU) is a rare Pediatric genetic disorder of inborn error of metabolism, where phenylalanine hydroxylase enzyme is deficient. This enzyme converts phenylalanine to tyrosie, which is required for melanin production and neurotransmitters of brain. Due to lack of enzyme, body gets accumulating phenylalanine. This affects how the ...
218 views
3 months ago
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