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Dual marker
My wife undergone dual marker test and NT scan in 12th week . The result for NT scan is CRL-58. 2 mm Nasal bone-3. 2 mm NT-1 Umbilical cord -3 vessels Fetal heart rate -170 Dual marker test report: Free beta hcg -85. 8 IU/L     2.73MoM PAAP-A- 1. 98IU/L                   0.65MoM Trisomy 21- 1:695 intermediate risk Overall observation is showing low risk The doctor is saying to go for NIPT as it is having intermediate risk , is it something to worry about as the doctor said the child may be having any chromosonal abnormality .
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Though 1 in 695 is a low risk, now we have a Noinvasive test called NIPT, in this scenario, better  do NIPT.
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Yes u should go for NIPT test
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It's only a prediction. Nobody can tell you for sure if baby will have chromosomal abnormalities or not. When you do NIPT or amniocentesis you will be able to get a more definitive answer.
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Double marker test is just a screening test Not a diagnostic test Intermediate risk needs further evaluation in the form of aminocentesis or nipt
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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.