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Trisomic 22 placenta in a case of severe intrauterine growth retardation
Authors:S Stioui  M de Silvestris  A Molinari  L Stripparo  L Ghisoni  G Simoni
Institution:1. Laboratorio di Citogenetica, Instituti Clinici di Perfezionamento, Milano, Italy;2. Clinica Ostetrica e Ginecologica, Università di Milano, Milano, Italy;3. Laboratorio di Citogenetica, Instituti Clinici di Perfezionamento, Milano, Italy

Clinica Ostetrica e Ginecologica, Università di Milano, Milano, Italy

Abstract:We describe a case in which a trisomic 22 placenta could be the cause of severe growth retardation in a chromosomally normal female fetus. At amniocentesis a mosaic 46,XX/ 47,XX, +22 was observed in amniotic fluid specimens sampled on two different occasions, while fetal blood from a diagnostic cordocentesis revealed a normal chromosome constitution. Postnatal studies showed the consistent presence of trisomic 22 cells in the placenta, while only normal metaphases were found in amnion, blood, and fibroblast cultures.
Keywords:Chorionic villi  Trisomy 22  Chromosomal mosaicism  Intrauterine growth retardation
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