EarlyPregnancy™ NIPT Plus Screen determines if singleton pregnancies have elevated risks for the most common chromosomal abnormalities in addition to microdeletion disorders and other rarer genetic disorders.
|22q11.2 deletion syndrome||1 in 4,000|
|1p36 deletion syndrome||1 in 5,000|
|Prader-Willi syndrome||1 in 10,000|
|Angelman syndrome||1 in 12,000|
|Cri du chat syndrome||1 in 20,000|
|Wolf-Hirschhorn syndrome||1 in 50,000|
There are many options available to you, once you’ve received your results. Our Board-Certified Genetic Counselors will help you understand your results in the context of your medical and family history. It is recommended that no irreversible clinical decisions be made based on these screening results alone.
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