phenylketonuria

     

Phenylketonuria (PKU) is an autosomal recessive genetic isorder characterized by a deficiency in the enzyme phenylalanine hydroxylase (PAH). This enzyme is necessary to metabolize the amino acid phenylalanine to the amino acid tyrosine. When PAH is deficient, phenylalanine accumulates and is converted into phenylpyruvate (also known as phenylketone), which is detected in the urine. PKU is found on chromosome number 12.

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  • Wow. PKU. It's been a long time. Really really long time. #Phenylketonuria
  • 시즌 1-5 [단백질 추적자] 페닐케톤뇨증은 PKU (phenylketonuria) 라고도 불린다.
  • It's been studied for decades, and consistently found safe for everyone, besides people with Phenylketonuria.
  • What if we could prevent mental illness with genetic screening? We do it for phenylketonuria, after all. David Mays:
  • Phenylketonuria or PKU: via @YouTube watch this small video and educate yourself on what PKU Please
  • @afrahtafri phenylketonuria
  • Phenylketonuria tisoy na bobo haha
  • Tisoy na bobo - phenylketonuria 😂😂😂😂😂
  • RT @KampusPsikologi: Fenilketonuria (Phenylketonuria) adalah gangguan desakan autosomal genetis yg dikenal dg kurangny enzim fenilalanin hi…
  • "Nurofen meltlets contain aspartame, which is a source of phenylalanine and may not be suitable for people with phenylketonuria." ...
  • Siap boleh tanya phenylketonuria lack of protein part mana. *terkedek-kedek selak lecture note
  • Fenilketonuria (Phenylketonuria) adalah gangguan desakan autosomal genetis yg dikenal dg kurangny enzim fenilalanin hidroksilase. #Psikologi
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