Abstract
We report a liveborn infant with severe intrauterine growth retardation and renal failure, delivered following detection of non-mosaic trisomy 2 by chorionic villus biopsy in the first trimester. Detailed analysis post-delivery indicated apparent complete trisomy 2 of the chorionic tissues, with a chromosomally normal infant demonstrating maternal uniparental disomy for chromosome 2.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Amniocentesis / adverse effects
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Chorionic Villi Sampling / adverse effects
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Chromosome Aberrations
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Chromosomes, Human, Pair 2*
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Female
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Fetal Growth Retardation / genetics*
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Fetal Membranes, Premature Rupture / diagnosis
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Fetal Membranes, Premature Rupture / etiology
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Fundoplication
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Gestational Age
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Hernia, Hiatal / surgery
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Humans
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Infant, Newborn
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Karyotyping
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Maternal Age
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Mosaicism*
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Placenta*
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Pregnancy
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Pregnancy, High-Risk
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Pyloric Stenosis / congenital
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Pyloric Stenosis / surgery
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Renal Insufficiency / diagnosis
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Renal Insufficiency / surgery
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Trisomy*
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Ultrasonography, Prenatal