Behind the Mystery Fragile X Syndrome: Genetic Disorder That Can Cause Learning/Behavior Challenges
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- Опубліковано 17 лип 2022
- Fragile X Syndrome is a genetic disorder that is caused by a gene mutation on the X chromosome. The symptoms frequently include developmental delays, intellectual disabilities, and behavioral issues. Carriers for Fragile X don’t have Fragile X syndrome; however, they do have an increased chance of certain medical issues as adults.
Screening for Fragile X is important, especially for individuals who are pregnant or plan to become pregnant. We spoke with Dr. Tamar Goldwaser, a medical geneticist, to learn more about screening for Fragile X, and Ilana Garber, a Fragile X Syndrome mom. To learn more, go to DiscoverFragileX.com.
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Wow montell Williams has to be at least 100 years old he was there when I was growing up lol
Wondering if the father has been tested as well. He may be a carrier also, which changes the probabilities as well.
Is it life threatening?
Whats the difference between fragile x and autism ?
Much more frequent in Ashkanazi Jews, as is FXTAS and Premature Ovarian Insufficiency Syndrome.
Too little research done on girls and women.
ashkan What? thats a contradiction they never got along is history being retconned now 😂
It comes from grandparents who died in Parkinson’s disease that is what fragile X syndrome come from.
Wow really
@@familyiseverything1617 Yeah sometimes it can be Idiopathic.
@@franzjosephaque2066 wow never knew that.... some of my family has it but not the grandparents.....
No, a granparent carrier has FXTAS.
Please be careful in your posts.