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.
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
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
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!
I am 42 years old and was diagnosed with 10% mosaic turners syndrome when my mother was still pregnant with me by amniocentesis. What that means is for every 9 normal cells in my body I have one cell that is fully or partial missing the second x chromosome (the sex chromosome). It is only in females and it can be a fluke. I have the wide spaced eyes, the lower and larger ears, and the short stature even though I am taller than most that have it (I am 4ft11). But instead of the narrowing of the aorta valve I have a click in mine that sounds like a squeaky door shutting. Due to TS I was never supposed to start my periods or develop breasts without estrogen shots (not supposed to be able to have children either) or be as tall as I am (even though it's short) without growth hormone shots, but being a child of a military family the military insurance wouldnt pay for them. I was very lucky I started my puberty on my own at 11 yrs old and even though I have had irregular periods ever since I was blessed with an amazing son that is now 15 years old and the best thing I have ever done. Dont get me wrong it was not easy on me, my mother (who was doing it all on her own as a single parent) was always there with me or my six older siblings (yes I'm the youngest of seven children) at home because I was in and out of hospitals seeing specialists and having surgery to correct different things that came with having TS. I've had two brain surgeries (due to front nasal encephalocele), 8 ear surgeries (including an ear drum rupture repair), 2 endoscopic sinus surgeries (including a reconstruction of my upper sinuses), my tonsils and adenoids removed, and wrist surgery to remove a cyst. That was all before 12 yrs old. Even though I have lived with Turner Syndrome my whole life I've always refused to let it defined me or my life. I have worked normal jobs from retail to offices work to being a corrections officer at a county jail. I am the example of dynamite comes in small packges. If you happen to want to learn more about Turners please read the book "Little things come in big packages" (I believe thats the name, but its been years since I've read the book. Or please do your own research on it because it isn't a syndrome that is talked about enough. Sorry for the rambling but i just had to comment on this clip.
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?
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❤️
The sperms can have either a x or y chromosome, u explained about a sperm having no chromosome fuses with a egg, results in turners syndrome. What if a sperm having a y chromosome fuses with a egg with no x chromosome .
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!
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
@@OranG_01 yep, and sometimes it isnt diagnosed until later too. i wasnt until i was a teen. now adays i think they can do more genetic screenings before hand and have gotten better with diagnosing things earleir though if the baby is born and they suspect
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
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.
I am a retired advanced theraputic endoscopist-gastroentgerologist. Excellant presentation. A very clear presentation for medical students and others.
Thank you for the feedback 🙏🏼 ❤️ 😊
"feels the same way" 😂
💀😂
😂😂
😂😂
👀👀🌚🌚
I was about to say the same😂😂
I have Turner’s syndrome and this video was very helpful, thank you! ❤
Always our pleasure to help, Lily! 🙏🏼
Same!!
Same situation with me
ur still a female, great to hear
All the best sister
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.
lost my baby girl to turner’s syndrome, was 11 weeks. thank you for this explanation ❤
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
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! 🥰❤️🙏🏼
I am 42 years old and was diagnosed with 10% mosaic turners syndrome when my mother was still pregnant with me by amniocentesis. What that means is for every 9 normal cells in my body I have one cell that is fully or partial missing the second x chromosome (the sex chromosome). It is only in females and it can be a fluke. I have the wide spaced eyes, the lower and larger ears, and the short stature even though I am taller than most that have it (I am 4ft11). But instead of the narrowing of the aorta valve I have a click in mine that sounds like a squeaky door shutting. Due to TS I was never supposed to start my periods or develop breasts without estrogen shots (not supposed to be able to have children either) or be as tall as I am (even though it's short) without growth hormone shots, but being a child of a military family the military insurance wouldnt pay for them. I was very lucky I started my puberty on my own at 11 yrs old and even though I have had irregular periods ever since I was blessed with an amazing son that is now 15 years old and the best thing I have ever done. Dont get me wrong it was not easy on me, my mother (who was doing it all on her own as a single parent) was always there with me or my six older siblings (yes I'm the youngest of seven children) at home because I was in and out of hospitals seeing specialists and having surgery to correct different things that came with having TS. I've had two brain surgeries (due to front nasal encephalocele), 8 ear surgeries (including an ear drum rupture repair), 2 endoscopic sinus surgeries (including a reconstruction of my upper sinuses), my tonsils and adenoids removed, and wrist surgery to remove a cyst. That was all before 12 yrs old. Even though I have lived with Turner Syndrome my whole life I've always refused to let it defined me or my life. I have worked normal jobs from retail to offices work to being a corrections officer at a county jail. I am the example of dynamite comes in small packges. If you happen to want to learn more about Turners please read the book "Little things come in big packages" (I believe thats the name, but its been years since I've read the book. Or please do your own research on it because it isn't a syndrome that is talked about enough. Sorry for the rambling but i just had to comment on this clip.
Excellent presentation! ❤
Thanks! ❤️
cannot thank you enough.Thank you so much for your clear and concise explanation!
You're welcome! 🥰
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! 💕
So helpful just before the night of my exam😊😍
We hope it went well! 🥰
اللهم صل وسلم وبارك على سيدنا محمد وعلى اله وصحبه اجمعين
Ameen❤
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 😊
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?
Amazing lecture
Thanks
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❤️
I have Turner syndrome too
The sperms can have either a x or y chromosome, u explained about a sperm having no chromosome fuses with a egg, results in turners syndrome.
What if a sperm having a y chromosome fuses with a egg with no x chromosome .
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
Great content 🤝
Thank you! 🙌🏼
simple and to the point. Many thanks
You're welcome, Yapa! 🙏🏼
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
@@OranG_01 yep, and sometimes it isnt diagnosed until later too. i wasnt until i was a teen. now adays i think they can do more genetic screenings before hand and have gotten better with diagnosing things earleir though if the baby is born and they suspect
Excellent explanation 👌
Thank you, Sara! 🙂
Amaaaazing ♥️♥️♥️♥️♥️♥️
Thank you so much 😊
You're welcome! 😊
Splendid explaination 👍🧡🤍💚
Thanks, Adhrithi! 😊
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
Excellent video, thank you!
You're welcome, Diana! 🙏🏼
3:31
Can men have that
No
Thank you good explanation 😊
You're welcome, Rupa! 😊
Awesome 😎 , it's most helpful for remember entire life
Glad to hear that, Asad! 💖
excellent
Thanks, Bella! 😊 💕
Yahh feel the same way 😂
Nice
Thank you, Maeraj! 💕
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.
What a stupid comment 😒
Excellent thanks for the details!
Our pleasure! 😊
6:32