Click through to uncover the in-depth disscussion, expert insights, and valuable context that paint the complete picture. Check out the full story to see the entire article.

Click through to uncover the in-depth disscussion, expert insights, and valuable context that paint the complete picture. Check out the full story to see the entire article.

In recent media cycles, there has been significant coverage focused on the rise in cancer cases among younger adults. It’s important to understand the complexities of this trend and what might be driving it, so people can be aware of their risks and take charge of their health.

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In late 2020, amidst a global pandemic and with the guidance of my GYN, I decided to do a hereditary cancer genetic panel that would test for over seventy known genetic mutations linked to all different hereditary cancers. My own mother is a breast cancer survivor. She was diagnosed at 40 years young but we were always told that because she did not have a BRCA mutation that the cancer wasn’t genetic. Being the daughter of a scientist and a survivor, this didn’t seem like the complete picture.

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What causes fragile X syndrome? Fragile X syndrome is caused by changes in the FMR1 gene found on the X chromosome. Typically, this gene produces a protein which is essential for proper brain development. In Fragile X syndrome, a part of the FMR1 gene is repeated too many times, resulting in reduced protein production that disrupts the normal brain function and leads to the characteristic symptoms of Fragile X. The number of repeats within the FMR1 gene impacts the severity of the condition.

Click through to uncover the in-depth disscussion, expert insights, and valuable context that paint the complete picture. Check out the full story to see the entire article.

Click through to uncover the in-depth disscussion, expert insights, and valuable context that paint the complete picture. Check out the full story to see the entire article.