*Department of Obstetrics and Gynecology,Slovak Medical University, 1st Private Hospital Košice-Šaca Inc., Košice-Šaca, Slovak Republic
**Charles University, Prague, 1st Faculty of Medicine and General Teaching Hospital, Department of Obstetrics and Gynecology, Prague, Czech Republic.
Case report
A 29-year-old G1P0 was referred to our department for an ultrasound scan at 24 weeks of gestation. She had non-contributive personal or family history. The first trimester screening was not done. Her triple test came out positive with a 1:85 risk for a trisomy 18. There was an intrauterine growth restriction (3 weeks delay of fetal growth).The ultrasound examination revealed the following findings:
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Hypoplastic nasal bone
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Micrognathia
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Choroid plexus cyst
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Bilateral radial aplasia
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Clenched fists
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Club-foot
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Intrauterine growth restriction
We suspected a chromosomal abnormality and performed an amniocentesis. Karyotype results showed Trisomy 18. Patient opted for a pregnancy termination.
Images 1,2: Image 1 shows a hypoplastic nasal bone, micrognathia. Image 2 shows a sagittal view of the fetal spine.