NIPT, NIPT-Plus（AssuriT-A/A+）
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NIPT（AssuriT-A）
Pregnancy can be exciting for families, and also bring concerns about medical decisions or the challenges of parenting. Prenatal screening offers genetic insights early in pregnancy about the health for the pregnant person and their growing baby.
NIPT plus（AssuriT-A⁺）
Research indicates that the prevalence of pathogenic copy number variations (pCNVs) in fetuses ranges from 1.6% to 1.7%, substantially exceeding the incidence rates of Trisomy 21, Trisomy 18, and Trisomy 13. Furthermore, pCNVs carry a high recurrence risk and represent a major genetic etiology of fetal congenital malformations, intellectual disabilities, and other birth defects.
