Fragile X Syndrome: Prenatal Detection, Timing, and Pregnancy Testing Explained | Dr. Shruti Bajaj

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Welcome to The Purple Gene Clinic! In this in-depth video, Dr. Shruti Bajaj discusses the critical aspects of diagnosing Fragile X Syndrome while the baby is still in the womb.
Are you detected to be a carrier for Fragile X syndrome?
Do you have a child with Fragile X syndrome, and are looking to plan another pregnancy?

Gain insights into why timely genetic testing is essential and learn about the specific timings of the same.

In this video, you’ll learn:
What is Fragile X Syndrome?
A brief overview of the main symptoms of Fragile X Syndrome
How Can Fragile X Be Detected during an ongoing pregnancy?

What Tests Are Conducted?
Explore the various genetic tests used for diagnosing Fragile X: including the FMR1 DNA test, prenatal testing, and carrier screening tests

When Should These Tests Be Conducted?
Understanding the timeline for testing, including prenatal and postnatal testing recommendations.

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Mam meri baby ko autism nai hai delay development me hai genetic test me chromosome 10 and 11 me translocation problem ai hai to plz iske bare me details se video dale iske kya kya symptoms hai or kitni age tak bacha normal ho sakta hai ya uske sath kya kya problems a sakti hai me apse mli hwi hu Dr- bharat pramar ne reffer kya tha apke pass

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