Starting in 2018, newborns in North Carolina will be able to undergo free screenings for genetic diseases. Although babies in America are tested for some genetic diseases, the screening doesn’t extend to all genetic disorders as the cost would be astronomical.
Up to 120,000 newborns in North Carolina will be eligible for the screenings and because the program is part of a research study, the company intends to follow up on any babies found to have SMA or fragile X syndrome and offer the families a chance to take part in further studies or participate in clinical trials. Find out more about the screenings here.
SMA News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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