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Abnormal pregnancy sonogram and chromosomal anomalies: Four years' experience with rapid karyotyping
Authors:M Hentemann  R Rauskolb  R Ulbrich  Dr I Bartels
Institution:1. Institut für Humangenetik, Göttingen, F.R.G.;2. Albert-Schweitzer-Krankenhaus, Northeim, F.R.G.;3. Universitätsfrauenklinik, Göttingen, F.R.G.
Abstract:Over a four-year period, 140 pregnancies with different malformations detected by ultrasound were examined cytogenetically. Gestational age ranged from 13 to 36 weeks. Twenty-six fetuses (18.6 per cent) had abnormal karyotypes, including trisomies, triploidy, monosomy X, and structural anomalies. Similar malformations were found in fetuses with different chromosomal anomalies, indicating that the types of malformations are not specific for particular chromosomal anomalies. Chromosomal analysis was performed on amniotic fluid culture and by direct karyotyping of placental biopsies. Direct karyotyping is suggested to be the most rapid approach, especially if sonographic anomalies are detected close to the 24th week of gestation, shortly before delivery, and in cases of significant oligohydramnios.
Keywords:Prenatal diagnosis  Cytogenetic abnormality  Rapid karyotyping  Placental biopsy
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