The tests revealed that the fetus also had mutations in the SMN1 genes in both chromosomes. The team intervened at 32-week gestation period by giving the mother risdiplam - a drug approved by the ...
A child with a rare genetic disorder — spinal muscular atrophy type I — was treated prenatally for the first time. Courtesy of Jakob Owens via Unsplash During an amniocentesis test, a long, thin ...
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