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ShortNasalbone4.9mm at 20w0days anomaly

2024-02-19 16:52:19
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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Answers (5)

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Pls connect for online consultation and advice

Answered2024-02-20 05:12:42

YESNO

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Please show to a foetal medicine specialist.

Answered2024-02-20 02:43:41

YESNO

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Share your anomaly scan report

Answered2024-02-19 16:56:21

YESNO

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Connect

Answered2024-02-20 05:46:33

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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

Answered2024-02-20 01:36:43

YESNO

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