Prenatal Diagnosis · 1995 · 80 citations · 12 references
Life SciencesGeneticsCytogeneticsHuman GeneticsPrenatal DiagnosisClinical CytogeneticsMolecular CytogeneticsPrenatal CytogeneticsPrenatal Genetic DiagnosisCytogenetic AberrationsFetal KaryotypingMolecular Cytogenetic DiagnosisMolecular Prenatal DiagnosisPeripheral Blood Lymphocyte AnalysisPrenatal Cytogenetic DiagnosisPrenatal Karyotyping
Fluid from pleural effusion (n = 2) and cystic hygroma (n = 7) was obtained from eight fetuses, between 13 and 32 weeks of pregnancy at the time when a conventional prenatal diagnosis procedure was carried out. As these fluids contain lymphocytes, they were processed like peripheral blood. A karyotype was obtained in 4 days in both cases of pleural effusion and in four out of seven samples of cystic hygroma. An abnormal karyotype was detected in three of the four samples of cystic hygroma: two trisomies 21 and a monosomy X. Different parameters were evaluated in order to predict the feasibility of obtaining a cytogenetic diagnosis. Our data showed that if the amount of fluid obtained was > or = 4 ml and the initial lymphocyte count (ILC) was > 0.2 x 10(6) cells/ml, a cytogenetic diagnosis was possible from an initial concentration of cultured lymphocytes (ICCL) of > 0.06 x 10(6) cells/ml.
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Frank A. Chervenak, Glenn Isaacson, Karin J. Blakemore et al. · New England Journal of Medicine · 1983 · 394 citations
Prenatal Diagnosis of Congenital Anomalies
Long-Term in Utero Drainage of Fetal Hydrothorax
Charles H. Rodeck, Nicholas M. Fisk, David I. Fraser et al. · New England Journal of Medicine · 1988 · 183 citations
Medicine, Obstetrics, Pediatrics +11
Prenatal Diagnosis and Screening
Journal of Medical Genetics · 1993 · 166 citations · Full text