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ShortNasalbone4.9mm at 20w0days anomaly
During my 20 weeks 0 days anomaly scan...we found short nasal bone of 4.9mm.
My Double marker test report showed low risk for T21 , T18 and T13 chromsomal abnormality test.
There was no ancestral case in both of husband or wife family for any abnormality.
Pls suggest should I go for NIPT test or amniocentesis or should I repeat scan in 1-2 weeks.
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Please show to a foetal medicine specialist.
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Dr. Neha Vashisth
Obstetrician
10 yrs exp
Jaipur
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Dr. Vijaya Gupta
Gynecologist
21 yrs exp
Chandigarh
There is no point going for nipt because that would again be a screening test with the higher sensitivity
You should connect with a genetic counselor
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Dr. Shruti Dahiya
Gynecologist
3 yrs exp
Delhi
Share your anomaly scan report
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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.