Human Reproduction · 1998 · 38 citations · 13 references
MedicineGeneticsObstetricsGenetic CounselingIn Vitro FertilizationInfertilityFemale InfertilityMale InfertilityPregnancyPreimplantation Genetic ScreeningPreimplantation Genetic TestingReproductive RiskChorionic Villi AbnormalitiesGenetic Abnormality AssessmentGenetic Risk ScreeningInfertility Risk PerceptionPregnancy Termination CounselingPregnancy-related TerminationPreimplantation Genetic Testing Decisions
Many couples undergoing in-vitro fertilization (IVF) are at a higher risk of having a child with a genetic abnormality. In a sample of 55 consecutive couples starting IVF, only 33% had no genetic risk factor. The most common genetic risks were advanced maternal age and possible abnormalities associated with severe male infertility. Despite education on these risks, 71% of couples had no interest in receiving formal genetic counselling. Only 14% of couples at risk would consider using a gamete donor to avoid transmitting a genetic disorder to a child. The triple test to screen for fetal abnormalities was acceptable to 82% of couples, but only 47% planned to have amniocentesis or chorionic villi sampling. Couples were significantly more likely to opt for prenatal testing if they would consider terminating a pregnancy should the fetus have a severe genetic abnormality (P < 0.01). Roman Catholic couples tended to have more conservative attitudes about pregnancy termination. Socio-economic status and whether the infertility factor was male or female were not predictors of a couple's attitudes.
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Microdeletions in the Y Chromosome of Infertile Men
Jon L. Pryor, Marijo Kent‐First, A. Muallem et al. · New England Journal of Medicine · 1997 · 493 citations · Full text
Cystic fibrosis mutation screening in healthy men with reduced sperm quality
K. van der Ven, Laurel H. Messer, H. van der Ven et al. · Human Reproduction · 1996 · 199 citations · Full text