* UVN SNP Ruzomberok, Gynekologicko-porodnicke oddelenie, Povazska 2, 034 01, Ruzomberok, Slovak Republic;
** Centrum prenatalnej diagnostiky, s. r. o., Masarykova 17/A, 040 01 Kosice, Slovak Republic.
Case report
A 21-year-old woman (G2P1) was sent to our unit at her 23rd week of pregnancy for an abnormal triple test. Her first trimester ultrasound was reported to be normal. Our ultrasound examination revealed following findings:
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Atrioventricular septal defect (complete form);
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Bilateral choroid plexus cyst;
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Short nasal bone;
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Prenasal edema (nuchal fold thickness was 5.1 mm - e. g. just close to the upper limit of 6 mm).
The findings were suggestive of chromosomal anomaly (especially trisomy 21) and amniocentesis with PCR testing was performed immediately. The results confirmed the diagnosis of trisomy 21.
Images 1, 2: The images show the four-chamber view of the fetal heart with the atrioventricular septal defect (AVSD). The image represents a fusion of the image1 with a drawing describing the visible structures.