By Keesha Harewood Global News
Posted on June 9, 2022 at 1:38 pm
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A newborn screening program at Cadham Provincial Laboratory is expanding its services to include spinal muscular atrophy (SMA).
According to the province, SMA is among the most common causes of deadly genetic disorders in children, occurring in approximately one in 18,000 babies.
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“Being able to expand our newborn screening program means faster, more accurate information and better options for Manitoba families,” said Dr. Paul Van Caeseele, medical director of Cadham Provincial Laboratory.
“SMA screening will diagnose babies before an irreversible disease occurs and connect them with early care that will give them a much greater chance of living an active and healthy life.”
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Muscular Dystrophy Canada will donate $ 235,000 to the lab over a two-year period to support the expansion.
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“Early diagnosis is key to improving the outcomes of babies born with metabolic, endocrine, or genetic disorders such as spinal muscular atrophy,” said Health Minister Audrey Gordon.
“Our government is proud to work with our healthcare partners to expand the newborn screening program to include SMA testing, because we know it is the first step in accessing treatment and ensuring the best outcomes for families.” .
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