Cell-free DNA screening
for trisomy 13, 18 and 21

Patient Space

A method for Cell‐free DNA screening for trisomy 13,18 and 21

This test is a method enabling, from a simple blood sample from the mother, to determine with a very high reliability if the fetus carries a trisomy 13, 18 or 21.

The document below contains the main information related to the Cell‐free DNA screening for trisomy 13,18 and 21.

nouveau test trisomie 21 patiente FRADownload the information brochure

 

Would you have any question, just ask your doctor monitoring your pregnancy or your clinical pathologist.


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