Abnormal: there is a strong suspicion of the presence of trisomy 21, 18 or 13 in the baby.Normal: there is no indication for the presence of trisomy 21, 18 or 13 in the baby.Please only contact us in case you have not received a result after 10 calendar days. In case of an abnormal result, one of our centers’ clinical geneticists will inform both you and your physician.You will also receive a hard copy of these results. The results can be consulted in your online medical file through ‘ mynexuzhealth’.In most cases, the result will be available after 7 to 10 calendar days counting from the receipt of the blood sample in our laboratory. However, the report only states the result for chromosomes 13, 18 and 21, unless an additional abnormality was found that is important for your own or your baby's health. NIPT analysis always involves a genome-wide analysis. Numerical abnormalities of the sex chromosomes (such as Turner syndrome or Klinefelter syndrome).Monogenic (single gene) disorders (such as cystic fibrosis or fragile X syndrome).Small chromosome abnormalities (microdeletions or microduplications), except for the few specific microdeletion syndromes mentioned above.Mosaic trisomy 21, 18 or 13 (not all the cells have a trisomy).Please note that NIPT is currently not able to detect all cases of these rare incidental chromosome abnormalities. In either one of these cases, one of our centers’ clinical geneticists will inform you and your physician accordingly and offer you the necessary multidisciplinary care.
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