High Incidence of Genetic Disorders Drives Prenatal and Newborn Genetic Testing Market

Genetic testing refers to the methodical diagnostic and screening techniques used to detect the possibility of genetic anomalies in unicellular and multicellular organisms. In particular, prenatal and newborn genetic testing refers to employing screening/diagnostic procedures to detect chromosomal abnormalities such as Patau syndrome, Edward syndrome, and Down syndrome in a fetus or a newborn. The technique comprises biochemical tests in order to identify the possible presence of genetic disorders or mutated genes that have higher risk of developing into genetic disorders later.

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