The first screening ultrasound plays a very important role in the diagnosis of congenital abnormalities and chromosomal syndromes. The most common chromosomal syndromes include trisomy 21, 18, and 13, whose symptoms are identified in the first screening ultrasound, in the form of non-standard thickness at the back of the fetus's neck. In the first screening, the fetus must be lying on the pelvic floor according to the standard criteria. If the standard cases are not met, the mother is forced to do additional tests. This ultrasound requires great skill and accuracy.

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