Sonographic findings in trisomy 9

Wade D. Schwendemann, Stephen A. Contag, Joseph R. Wax, Richard C. Miller, William J. Polzin, Patrick P. Koty, William J. Watson

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Objective. The purpose of this study was to identify the most common prenatal sonographic findings in fetuses with complete trisomy 9. Methods. A retrospective review of all cases of trisomy 9 at 5 participating institutions over a 15-year interval was conducted. Indications for referral and sonographic findings in each case were reviewed to identify characteristic fetal structural anomalies. Results. Six cases of trisomy 9 are presented. Most patients were referred for abnormal sonographic findings on screening examinations (66%) or advanced maternal age (33%). Fetal heart defects and central nervous system malformations were the most frequent sonographic anomalies seen. Conclusions. Sonographic findings in trisomy 9 are similar to those found in other autosomal trisomies. Because trisomy 9 is uniformly lethal and is not included as part of the standard prenatal aneuploidy screening by fluorescence in situ hybridization analysis, clinicians should be cautious in counseling patients with structurally abnormal fetuses until the full karyotype is available.

Original languageEnglish (US)
Pages (from-to)39-42
Number of pages4
JournalJournal of Ultrasound in Medicine
Volume28
Issue number1
DOIs
StatePublished - Jan 1 2009

Keywords

  • Prenatal diagnosis
  • Sonography
  • Trisomy 9

Fingerprint Dive into the research topics of 'Sonographic findings in trisomy 9'. Together they form a unique fingerprint.

Cite this