Andrea Vaskova, MD.
Presov, Slovak republic
Case report
31-year-old woman (G4P3) with non-contributive history, from non-consanguineous couple, presented to our facility at 17 weeks of pregnancy. She did not undergo first trimester ultrasonographic  NT screening, but her biochemical triple test was normal.
Our ultrasound examination revealed micromelia and short narrow thorax of the fetus. The patient had refused amniocentesis. Her following ultrasonographic scans were performed between 22 and 31 weeks of pregnancy. They revealed macrocrania with abnormal cloverleaf shaped skull, frontal bossing, low nasal bridge, low-set ears, narrow bell-shaped thorax with relative cardiomegaly, prominent abdomen, platyspondyly, trident hands, hypoplastic iliac bones, and polyhydramnios. Our presumed diagnosis was thanatophoric dysplasia type II.Â
The patient opted for the continuation of the pregnancy. The newborn was delivered via cesarean section at 35 weeks due to massive polyhydramnios and threat of uterine rupture because of previous cesarean section.
The findings and diagnosis were confirmed postnatally. The newborn died four hours after delivery.
Images 1, 2: 17 weeks of pregnancy: the images show short femur and tibia of the fetus (Image 1) and short narrow fetal thorax (Image 2).