Video

How is Fragile X Syndrome Inherited?

00 h 02 m

How Fragile X syndrome is 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.

About the Video

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 about 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.

Additionally, once an individual or parent receives a diagnosis, talking about it with potentially affected family members can be difficult for many reasons. If this is you, we have resources to help families with a new diagnosis. We hope this quick video will help you better understand how Fragile X is inherited.

Additional Resources

About the Narrator

Dan Whiting

Dan served as the NFXF Director of Community Impact from 2017 to 2022. He has over 23 years of experience in public policy and communications, including 11 years as a staff member for a U.S. Senator, in the Bush Administration as Chief of Staff at an agency, and as a senior strategist for communication initiatives across the DOD. During his time at the NFXF, he was passionate about helping individuals with intellectual and developmental disabilities live better lives.