Chromosomal markers found in my NT scan report is nasal bone length is short 2.7 mm and Trisomy 21 background risk 1: 565 and adjusted risk 1: 17. Final comment like nasal bone appears hypoplastic. Could you please suggest us is there any issue?
Suggest to seek fetal medicine opinion, all your reports will need detailed review and you may be asked for amniocentesis to confirm possibility of downs syndrome in baby.book teleconsult to discuss further
Here is the dual marker and NT scan report for my wife. Can you suggest if its normal or we need NIPT sca
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