New England Journal of Medicine · 1981 · 83 citations · 11 references
MedicineGeneticsObstetricsMaternal-fetal MedicineMedical GeneticsPrenatal DiagnosisCongenital AnomaliesCongenital DisordersCongenital MalformationsFetal AnomaliesFetal Anomaly DetectionCongenital Anomalies GeneticsCongenital Malformation DetectionFetal Chromosomal AbnormalitiesPrenatal Diagnosis Of Down SyndromePrenatal Diagnostic TestingTwin Pregnancy ScreeningTwin Pregnancy Testing
AMNIOCENTESIS for genetic evaluation is now a well-established prenatal diagnostic procedure. The discovery of twins at the time of amniocentesis, however, necessitates additional measures, and in the event of detection of discordancy for an abnormality, it poses a challenging problem. In 1975, Bang et al. reported the first successful amniocentesis and karyotyping in twins. They also forecast the inevitable dilemma: "One unsolved question is the consequence of finding one abnormal and one normal fetus."1 At least five recent articles have described cases in the mid-trimester in which one fetus had a major congenital malformation and the other one was normal. . . .
11
Congenital malformation in twins.
P M Layde, Jon D. Erickson, Arthur Falek et al. · PubMed · 1980 · 104 citations
Medicine, Genetics, Pediatrics +12