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What are the recommended genetic tests for Cerebral Palsy diagnosis?

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Dr.Prajnya Ranganath

Also available in: हिंदी
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Key Takeaways:

  1. Most cases of Cerebral Palsy (CP) are not genetic in origin.
  2. CP commonly occurs due to physical injury, lack of oxygen, or poor blood flow during pregnancy.
  3. Pregnancy scans and Doppler studies help detect growth issues or oxygen/blood supply problems in the fetus.
  4. Some neurodevelopmental disorders caused by genetic defects may be mistakenly labeled as CP.
  5. Accurate diagnosis is crucial, since other genetic or neuro-developmental conditions can mimic CP symptoms.

Most individuals with Cerebral Palsy do not have a genetic basis for its occurrence. Cerebral Palsy most commonly occurs due to physical injury or lack of blood flow or oxygen during pregnancy. Pregnancy scans and Dopplar studies can be recommended to identify growth defects, physical injury or lack of oxygen/blood supply to the foetus. Some children with neuro-develpmental defects (which are linked to gene defects) can be mislabeled as having Cerebral Palsy. Confirming a diagnosis for Cerebral Palsy is very important, as other neuro-developmental disorders can be mislabeled as Cerebral Palsy.

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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