Turner syndrome (Year of the Zebra)
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- čas přidán 18. 02. 2023
- What is Turner syndrome? Turner syndrome, named after Henry Turner who first described it, is a chromosomal disorder affecting females where one X chromosome is either completely or partially absent.
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"feels the same way" 😂
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I have Turner’s syndrome and this video was very helpful, thank you! ❤
Always our pleasure to help, Lily! 🙏🏼
Same!!
I am a retired advanced theraputic endoscopist-gastroentgerologist. Excellant presentation. A very clear presentation for medical students and others.
Thank you for the feedback 🙏🏼 ❤️ 😊
I like the refresher. My kid is 14 so we have been managing this for a while now. She has started the hormonal growth therapy. Almost daily shots so between that and the cost ( thank goodness for the financial assistance) we have our hands full. It's still pretty early in development but Doc said might have to start the estrogen treatment if she wants to hv a shot at kids and more adult development. She did have open heart surgery as a baby,she did great!. And another one if in the near horizon as she grows into an "adult sized heart" Doc says. Not looking forward to that one. The impact definitely feels different.
As a woman who is trying to find true research or info and understandable info on genetics (which is a puzzle In itself even for the geneticists) thank you for all geneticists with what you do! Anyways I am a woman with possible Turners so this really helped me with good info but true info!
We're happy that our video was able to help! 🥰❤️🙏🏼
Thank you ❤
Very helpful information. How much certainty should be given to an NIPT screen showing a very high percentage of Turners? I know only way is an amnio test, but if an NIPT shows it, is it fairly accurate most of the time?
My daughter has TS and is now 39, when diagnosed she was 11 & had growth hormome(synthetic)& thankfully it was the synthetic hormone, I personally still don't understand, thank you for this video ,
Keep Lifted
We hope this video helped, Karen 🙏🏼
My daughter is 38 and was diagnosed after her birth. She had the synthetic hormone injections and is 5' 2. She presents okay with people not realising. However she also has high functioning autism. She drives and works part time. Her kidneys and heart are fine. She does have hypothyroidism but so do I. She is pre diabetic. Life with her is not a bed of roses at times, and she has no desire to live on her own. Still she stays reasonably healthy and that's good
Excellent presentation! ❤
Thanks! ❤️
اللهم صل وسلم وبارك على سيدنا محمد وعلى اله وصحبه اجمعين
Amazing lecture
Thanks
Our pleasure 🙏🏼
simple and to the point. Many thanks
You're welcome, Yapa! 🙏🏼
Great content 🤝
Thank you! 🙌🏼
The pun included during narration of this video and the majority of your videos is joyful 😄
We're glad that you're enjoying our videos, Wael! 💕
Excellent video, thank you!
You're welcome, Diana! 🙏🏼
Amaaaazing ♥️♥️♥️♥️♥️♥️
I have Turner syndrome too
thank you for making this useful presentation, but how can we see the references?
Hi! You may get in touch with our team via email at support@osmosis.org 😊
Excellent thanks for the details!
Our pleasure! 😊
i am actually confused about one thing - you said that during mosaicism these cells that have 47 chromosomes doesn’t survive but i remember that in the other video about dawn syndrome man said that its 45 chromosomal cells that doesn’t survive.
guess i missed something 😆 but thank you anyway it was really helpful❤️
Excellent explanation 👌
Thank you, Sara! 🙂
I am 17 years old .. I had my period when I was almost 12 years old and completely regular , but I am short my height is 153 cm , and my weight is 37 kg . My intelligence is very normal , and I look much younger than my age also my body showed no signs of puberty .. I do not have the rest of the symptoms. Can anyone help me to know if I have Turner syndrome ?
Hello, you need to go to your DR and ask for a “katyotype” test. This is super simple and fairly painless. All they do is take some blood and look at the cells. I wish you the best!
@@Peculiarimmigrant36 Thank you very much 💗
As someone with Turners, I would say maybe. Usually if you have turners you don’t get periods without hormone replacement, but sometimes they start normally then stop in early adulthood. I would definitely get checked out, regardless if it was Turners or not. Maybe it’s something else entirely or nothing at all
Splendid explaination 👍🧡🤍💚
Thanks, Adhrithi! 😊
Thank you good explanation 😊
You're welcome, Rupa! 😊
So what is the product that can literally trigger a turber syndrome
It’s from birth, you are born as a turner female
So the best way to check if u have turner is to see your karyotype
Awesome 😎 , it's most helpful for remember entire life
Glad to hear that, Asad! 💖
3:31
6:32
A man with 45 chromosomes?
Where is information on this man.
A carrier for Down Syndrome and also Infantile Neuroaxonal Dystrophy.
Please help with information
Can men have that
No
excellent
Thanks, Bella! 😊 💕
Nice
Thank you, Maeraj! 💕
Yahh feel the same way 😂
3RD GENDER
Sorry, but we are not 3rd gender! We are women with maybe health problems, but live a life as other women...so please think before you say something like this.