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Genetics of Stillbirth

23 Jul 2010

Abstract excerpt

Approximately 25% of stillbirths have been attributed to genetic etiologies. The most common cytogenetic abnormalities are similar to those seen in liveborns and include 45X, trisomy 21, trisomy 18, and trisomy 13. Cytogenetic abnormalities are more common when fetal structural anomalies are identified. Mendelian and metabolic causes of stillbirth are less well understood although single gene disorders can result...

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Share to Assisted Reproductive Technology and Twin Pregnancy
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 20661047
DOI: 10.1097/grf.0b013e3181ee2793

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