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Aminocentisis
My NT was 3.2 mm nasal bone was present during NT scan and dual marker test is low risk 1:350, suggested early anomaly at 16 weeks in that scan they are saying hypoplastic nasal bone of. 2.4 mm and suggesting for aminocentisis test. Please suggest me what i can do
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Go with NIPT  first Then u can
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Yes amniocentesis and karyotyping is confirmatory test to rule out Chromosomal anomalies
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Yes .. you need further evaluation. Actually your first trimester screening was also in intermediate risk.
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Disclaimer : The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.