Sifakis S, Koukoura O, Mantas N, Velissariou V, Koumantakis E
Department of Obstetrics and Gynecology, University Hospital of Heraklion, Heraklion, Greece.
Fetal Diagn Ther. 2008;24(3):310-2. doi: 10.1159/000160218. Epub 2008 Oct 3.
We report a case of trisomy 21 mosaicism detected upon amniocentesis in a 36-year-old woman. Ultrasound examination at 23 weeks' gestation showed a fetus with hydrops, pulmonary hypoplasia, oligohydramnios, thickened placenta, and intrauterine growth retardation. Cytogenetic analysis revealed low-percentage (6%) mosaicism for trisomy 21. Hydrops fetalis and thickened placenta are uncommon findings in fetuses affected by trisomy 21 mosaicism. A short review of the literature is given regarding the sonographic findings associated with trisomy 21 mosaicism, and the genetic counseling in such cases.