Phenylketonuria (Inborn Error of Metabolism) for USMLE

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  • Опубликовано: 8 ноя 2024

Комментарии • 13

  • @feliciayodiutama6527
    @feliciayodiutama6527 4 года назад

    Thank you very much for the video. It helps me to understand a lot more about my child who is born with BH4 deficiency (PTPS deficiency specifically).

  • @wahidexplains
    @wahidexplains 5 лет назад

    Very good video on PKU yet

  • @maramal-shahrani1956
    @maramal-shahrani1956 7 лет назад

    very informative and nice presentation

  • @magdahassan8052
    @magdahassan8052 Год назад

    Thanks' alot...

  • @marvoht
    @marvoht 8 лет назад

    Excellent video. Can you explain why you would supplement them w/ Phenylalanine if they already have excessive amounts of it?

    • @thestudyspot
      @thestudyspot  8 лет назад +5

      +tee h You wouldn't supplement Phenylalanine, you would restrict phenylalanine. That is important to prevent progression of the disease. However, you do need to supplement Tyrosine because there is no other way for you body to produce Tyrosine without Phenylalanine as a precursor.

    • @marvoht
      @marvoht 8 лет назад

      .

    • @marvoht
      @marvoht 8 лет назад

      the study spot right, what i meant is that why would their diet consist of 20-30mg/kg/day of Phenylalanine when they already have excessive amounts of it..

    • @marvoht
      @marvoht 8 лет назад

      b/c we are currently learning about it & I came across that in my slides & was a bit confused

  • @danaghazaleh9117
    @danaghazaleh9117 9 лет назад +1

    Very comprehensive :)

  • @melissaarana4933
    @melissaarana4933 9 лет назад

    Do people with hi levels or Phenylketonuria in there blood do they experience a lot of food sensitivities ? Please let me know very important to my experiences….

    • @thestudyspot
      @thestudyspot  9 лет назад

      +Melissa Arana I haven't come across anything that makes such a link.

  • @عامرحسين-و7ح
    @عامرحسين-و7ح Год назад

    Hello i have 2 questions, first why phenylketonuria cause mental retardation microcephaly and mousy odor, second is dopamine differentiatate types phenylketonuria, is dopamine has link with phenylketonuria