What is Fragile X Syndrome?
What is Fragile X Syndrome?
Nov 19, 2009
news-medical.net
How is Fragile X syndrome inherited is a very common question and one of the first things a newly diagnosed family asks. Let’s be clear – Fragile X is an inherited condition. With a very rare exception, when the FMR1 gene is deleted, the gene mutation came from either the individual’s father or mother. However, we all don’t talk genetics every day, so it can be a hard concept to follow. In fact – surprisingly – we still hear of doctors incorrectly stating how the gene mutation is passed down. Ad
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2K views · 18 reactions | Fragile X is a genetic disorder that affects 1 in 4,000 men. We are currently enrolling men with fragile X for a study at the NIH Clinical Center. Watch this short video to learn more about the study. Email: loutaev.inna@nih.gov or call 1-301-496-4707 [TTY: 1-866-411-1010]. | National Institute of Mental Health | Facebook
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