Hi
My daughter was born on 1st Dec 2020 and till now she hasn't been screened for any anomaly. Meaning, no tests are conducted.
I plan to go for following tests proactively:
G6PD
Thalesemia
Sickle cell Anemia
Phenylketonurea
Galactosemia
S. Bilirubin
Phenylalanine
Cystic Fibrosis
17-Hydroxy progesterone
Biotinidase
I want to know if I am already late to get these tests done? Some people told me that these tests shall be conducted within 48-72 hours of baby birth.
Would it be fine if I still go for these tests?
Last question, please let me know if any of the above test is not important or if I missed any crucial test?
Thanks
Answers (4)
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What is the reason for your thinking of these tests ? If you have family history a systematic plan can be decided for you which may have even other tests than what you are thinking of. So be specific please .
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These tests may be suggested as a part of New born screening. It can be done anytime before discharge ideally. Do TSH or Thyroid profile also along with them.
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Disclaimer : The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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