First-trimester prenatal diagnosis of Roberts syndrome
- PMID: 1553361
- DOI: 10.1002/pd.1970120211
First-trimester prenatal diagnosis of Roberts syndrome
Abstract
We present a case of prenatal detection of premature centromere separation on chorionic villi sampled at 8 weeks' gestation from a woman at risk of recurrence of Roberts syndrome. The same cytogenetic characteristic was confirmed on amniocytes at 14 weeks when ultrasound examination showed morphological anomalies of the fetus. To our knowledge, this is the first report of early prenatal diagnosis of Roberts syndrome.
Comment in
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Prenatal diagnosis of Roberts syndrome.Prenat Diagn. 1992 Nov;12(11):976. doi: 10.1002/pd.1970121123. Prenat Diagn. 1992. PMID: 1494554 No abstract available.
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