Trisomy 9 In Prenatal Diagnosis - Case Report

• Authors: Małgorzata Soroka , Maciej Słodki
• Languages of publication: EN

Abstracts

EN

Trisomy 9 is a rare chromosomal disorder that often results in significant mortality. We present a case report in a low-risk pregnancy. The prenatal ultrasonography at 12 weeks of gestation showed normal nuchal translucency and the presence of the nasal bone. The anatomy scan performed by an experienced doctor revealed an abnormal four chamber view and abnormal posterior cranial fossa. First trimester biochemical analysis ( free βhCG and PAPP-A) showed high risk for trisomy 18. By amniocenthesis ( at 16 weeks of gestation ) and karyotype evaluation trisomy 9 was diagnosed and at 20 weekstermination was conducted on maternal request.

Keywords

EN

trisomy 9; prenatal ultrasound; Dandy-Walker malformation (DWM); horseshoe kidney; echocardiography

• Publisher: De Gruyter Open
• Journal: Prenatal Cardiology
• Year: 2014
• Volume: 4
• Issue: 1
• Pages: 24-28

Dates

published

1 - 3 - 2014

received

16 - 3 - 2014

online

30 - 12 - 2015

accepted

31 - 3 - 2014

Contributors

author

Małgorzata Soroka

• Department of Obstetrics and Gynecology - Hospital St. Trinity in Plock

author

Maciej Słodki

• Department of Obstetrics and Gynecology - Hospital St. Trinity in Plock,
• Department of Prenatal Cardiology, Polish Mother’s Memorial Hospital Research Institute,
• Institute of Health Sciences. The State School of Higher Professional Education in Płock

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Identifiers

DOI

10.12847/03145