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VitaPath Genetics is sponsoring collaborative research with leading academic institutions to improve our understanding of the genetics of spina bifida, with the hope of developing a simple DNA test to identify women with an elevated of risk for this preventable birth defect. We are seeking mothers of children affected by Spina Bifida and their children to provide a saliva sample for validation of our genetic test. We are also recruiting mothers who have had children not affected by spina bifida to serve as controls for our study.

I have a child with spina bifida

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I do not have a child with spina bifida

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Spina Bifida

Spina bifida is the most common debilitating birth defect in the United States, affecting more than 3,000 families each year. Our research suggests that one of the causes of spina bifida may be a set of mutations in genes that require folic acid, and that preventing spina bifida in these cases may require prescription forms of folic acid supplementation prior to conception.

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Meet Our Team

The Spina Bifida Genetics Research Project is a collaboration involving researchers from the following organizations:

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What our participants & PARTNERS have to say about us:

I am so thankful to VitaPath for their commitment to learn more about Spina Bifida and its cause. My son and I participated in the first round of research conducted by VitaPath in their efforts to understand the genetic link to Spina Bifida. When I first told my son we were participating, he was nervous, because he thought the test might be uncomfortable. When we received the test in the mail, and he realized that it was only a swab, he was relieved. After finishing the swab, he asked, “Is that it? That was easy!” The swab test only took less than five minutes to complete. VitaPath also made returning the test to them incredibly easy. We were proud to be a part of such important research.
Angie Pate, mother of child with spina bifida
Deciding to participate in this study was a no-brainer for my husband and I. After our son was born, we became dedicated to changing the face of Spina Bifida. One way we could help make a difference, small as it may be, was to contribute to this study to help determine the cause of Spina Bifida. It was a very quick, simple process but yet will hopefully one day make a huge difference.
Michelle Dugan, mother of child with spina bifida