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Why is new born genetic screening necessary?

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Dr.Prajnya Ranganath

Also available in: हिंदी
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Key Takeaways:

  1. Newborn genetic screening detects metabolic disorders early.
  2. These disorders cause a buildup of harmful chemicals affecting brain development.
  3. Early detection enables timely treatment, preventing brain damage.
  4. Common metabolic disorders include Hypothyroidism, Phenylketonuria, and Galactosemia.
  5. Screening is simple and lifesaving, using a small blood sample from the baby.

Certain genetic disorders can cause increase in certain chemicals in the body which can affect brain development. These disorders are called Metabolic disorders. The baby’s blood can be screened for metabolic chemicals that can cause these metabolic disorders in the baby early on through New born metabolic screening. Early identification of metabolic disorders can permit early treatment and prevent potential brain damage. Hypothyroidism, Phenylketouria, Galactosemia are some common examples of metabolic disorders

DISCLAIMER: Please note that this guide is for information purposes only. Please consult a qualified health practitioner for safe management

If you have questions about Autism, Down Syndrome, ADHD, or other intellectual disabilities, or have concerns about developmental delays in a child, the Nayi Disha team is here to help. For any questions or queries, please contact our FREE Helpline at 844-844-8996. You can call or what’s app us. Our counselors speak different languages including English, Hindi, Malayalam, Gujarati, Marathi, Telugu, and Bengali.

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