What Is Edwards Syndrome | Testing For Edwards Syndrome

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  • Опубликовано: 15 окт 2024

Комментарии • 14

  • @lisa-mariegray5510
    @lisa-mariegray5510 Год назад +2

    Hi, Dr Papa. My son was stillborn at 23 weeks gestation almost 30 years ago. He had Trisomy 18. This is a very interesting video and I thank you for talking about these precious babies.

  • @kimsordyl
    @kimsordyl 2 года назад +3

    So informative and easily explained! Thank you Dr. Papa.

  • @Snail320
    @Snail320 3 года назад +3

    Great job, doctor!

  • @anisabwahab6191
    @anisabwahab6191 3 года назад +1

    good explaination. its easy to understand. thank you for making my life easier

  • @MissTotos
    @MissTotos 3 года назад +2

    I went through this. My fetus had severe hydrocephalus, a growth in a kidney and a heart defect.

    • @DrTracyPapa
      @DrTracyPapa  3 года назад

      I'm so sorry, it must have been scary for you. We all worry about how things will turn out - will the baby suffer? Will they need help breathing or eating? Every baby with trisomy 18 is different. I hope you had a provider and family and friends who helped you.

  • @angelorbeta4273
    @angelorbeta4273 2 года назад

    My baby have trisonomy 18. She is have a congenital diagphramatic hernia. She is 8 months old.

  • @branthoward5802
    @branthoward5802 3 года назад

    Hello. Thank you for posting this video. We just got our quad test results back and are high risk for trisomy 18 with a 3.24 reading over a 2.5 cutoff and are now in process of continuing on to our next appointment. I don’t understand the 2.5 cutoff baseline or if our reading is a lot higher then it sounds. Is that an super high reading over the Standard 2.5 baseline? Thank you for your video.

    • @DrTracyPapa
      @DrTracyPapa  3 года назад

      The quad test is based on measuring four different serum analytes in your blood. Remember that "increased risk" on a quad screen means your risk of trisomy 18 is higher than that of a 35 year old patient, which is about 1 in 500. So if your test reports that your risk is elevated, that may mean less than a 1% risk!
      When the test reports an increased risk of trisomy 18, the next step is usually a detailed fetal ultrasound to look for abnormalities that are associated with trisomy 18. You may be offered a secondary screen like NIPT, and should also be offered diagnostic testing. This means amniocentesis.
      Your provider will explain all of this, but don't worry too soon!
      Best of luck,
      Tracy

    • @branthoward5802
      @branthoward5802 3 года назад

      @@DrTracyPapa Thank you. Our screening test said 1/10 for trisomy 18. AFP was 3.24 Shes 29 years old. Our appointment is tomorrow morning so I’m hoping it’s nothing serious but thank you again for your reply

  • @tanyache215
    @tanyache215 2 года назад

    Hello. İ had ultrasound at 22 weeks. Doctor found out that baby has VSD 1.9 mm and coral plexus cyst. And also one thing that i am worry - baby never bend his legs. All others seems fine. And doctor told - dont worry, everything is good. But İ heard these could be symptoms of trisomy 18. Could you be so kind to give me advice what are my next steps, what need to do?

  • @ferreiramarelin6919
    @ferreiramarelin6919 8 месяцев назад

    I have trisomy 8