Literature DB >> 14992360

Second-trimester sonography and trisomy 18.

Richard Bronsteen1, Wesley Lee, Ivana M Vettraino, Raywin Huang, Christine H Comstock.   

Abstract

OBJECTIVE: This report presents the findings seen on initial second-trimester sonography in a large group of fetuses with trisomy 18. The object of this study was to describe the types and frequencies of abnormal sonographic findings seen and to further evaluate those cases in which no abnormal findings were noted.
METHODS: A retrospective chart review of the prenatal sonograms in cases of trisomy 18 was conducted.
RESULTS: Forty-nine fetuses with trisomy 18 were examined by second-trimester sonography. Multiple fetal anomalies were seen in most cases. The most frequent structural findings involved the brain (82%), heart (55%), and upper extremities (53%). Growth abnormalities occurred in 39% of these fetuses. Choroid plexus cysts were the most common individual findings. Larger cysts increased the likelihood of trisomy 18, although no fetuses with trisomy 18 had isolated choroid plexus cysts. Seven fetuses (14%) had no anomalies seen on their initial scans. In each of these scans, the fetal anatomy was incompletely visualized because of technical constraints. Six had subsequent scans approximately 2 weeks later, which showed abnormal sonographic findings.
CONCLUSIONS: Most fetuses with trisomy 18 were identified by structural anomalies, typically seen in the brain, heart, and upper extremities. Larger choroid plexus cysts were associated with this aneuploidy. Technical factors, which limit fetal visualization, were noted in all cases in which no sonographic abnormalities were detected during the initial sonographic examinations. Detection of abnormal cases will rely on a completed evaluation of a routine fetal anatomic survey.

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Mesh:

Year:  2004        PMID: 14992360     DOI: 10.7863/jum.2004.23.2.233

Source DB:  PubMed          Journal:  J Ultrasound Med        ISSN: 0278-4297            Impact factor:   2.153


  5 in total

1.  Prenatal diagnosis of i(18q) and dup(18q) cases by quantitative fluorescent PCR.

Authors:  Isabel Castro-Volio; Fernando Ortíz-Morales; Luisa Valle-Bourrouet; Wendy Malespín-Bendaña
Journal:  BMJ Case Rep       Date:  2013-09-17

Review 2.  A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Authors:  Anne H Mardy; Shilpa P Chetty; Mary E Norton; Teresa N Sparks
Journal:  Prenat Diagn       Date:  2019-06-26       Impact factor: 3.050

Review 3.  Microcephaly: a radiological review.

Authors:  Ailbhe Tarrant; Catherine Garel; David Germanaud; Thierry Billette de Villemeur; Cyril Mignot; Marion Lenoir; Hubert Ducou le Pointe
Journal:  Pediatr Radiol       Date:  2009-05-13

Review 4.  The role of ultrasound in the diagnosis of fetal genetic syndromes.

Authors:  Shayna N Conner; Ryan E Longman; Alison G Cahill
Journal:  Best Pract Res Clin Obstet Gynaecol       Date:  2014-01-28       Impact factor: 5.237

Review 5.  Trisomy 13, 18, 21, Triploidy and Turner syndrome: the 5T's. Look at the hands.

Authors:  G Witters; J Van Robays; C Willekes; A Coumans; H Peeters; W Gyselaers; J P Fryns
Journal:  Facts Views Vis Obgyn       Date:  2011
  5 in total

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