We just received our NIPT results and the results have us worried..
It said "Missing chromosome 21, parental cause due to abnormal sperm".
The doctor hasn't been able to say much other than she said the test may be wrong. I've seen other NIPT results with % chance or fraction chances but none like ours. Monosomy 21 is also a very rare disease.
My baby also has a high NT of 3.3 mm. In the ultrasound, the doctor said the baby is small but looks healthy. Im scheduled for amnio in 2 weeks but am seeking help from anyone with information on such diseases.