u/salsaespecial31

Unborn child is diagnosed with TOF. We don't know the full extent yet since we have more follow ups. We are 29+ weeks at this point. We have already done a genetics test (NIPT) and have come back negative on everything. With this new information, we are now extra worried that maybe 22q11 deletion syndrome might be something our child has. We are most likely going to do an amniocentesis test, but I wanted to hear from others to see if their child with TOF had this syndrome, even though their genetics test came back all negatives.