Donetsk`s regional specialized center of medical genetic and prenatal diagnosis, Ukraine.
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Case report
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A 40-year-old G3 P1, a Caucasian woman with uncomplicated previous pregnancy and 1 spontaneous abortion, was referred to our center for the ultrasound examination.
On our ultrasound examination at 18 weeks we revealed the following:
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Absent nasal bone
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Abnormal facial features: depressed nasal bridge, upslanting palpebral fissures, prominent zygomatic arches
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Clinodactyly of the little fingers
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Short big toes
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Aberrant right subclavian artery [1,2]
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There were no gross anomalies detected. We suggested amniocentesis based on the above findings. The karyotype result confirmed trisomy 21. The parents opted for the termination of the pregnancy.
The detection of the aberrant right subclavian artery seems to be useful tool in cases of suspected chromosomal anomaly. Presence of the aberrant right subclavian artery is much more common in fetuses with chomosomal defects than in fetuses with normal karyotype. The recent study of 2799 fetuses conducted in England showed that aberrant artery was present in 29% of fetuses with trisomy 21, 18% of cases of trisomy 18 and 8% of other chromosomal abnormal cases [2]. The presence of the aberrant subclavian artery maybe associated with cardiac anomalies as well. [2]
Images 1,2: Image 1 shows fetal profile, note absent nasal bone and prefrontal edema. Image 2 shows absent nasal bones.