Abstract:A 20-year-old primigravida was referred due to increased risk of trisomy 21 in the triple test result at 21 weeks of gestation, which was 1/59. Sonographic examination revealed hypoplastic nasal bone (NB=4.3 mm) and hyperechogenic bowel with mildly dilated segments (bowel diameter=4.5 mm) (Figure 1). Past medical histories of both parents were insignificant. There was no consanguineous marriage. Amniocentesis was performed. Quantitative fluorescence polymerase chain reaction (PCR), karyotype, and cystic fibros… Show more
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