Literature DB >> 25569015

Jacobsen syndrome detected by noninvasive prenatal testing.

Jamie O Lo1, Cori D Feist, Jason Hashima, Brian L Shaffer.   

Abstract

BACKGROUND: Noninvasive prenatal testing has a high detection rate of common fetal chromosomal aneuploidies. However, detection of additional chromosome abnormalities has not been well described or validated. CASE: We report a case of Jacobsen syndrome, a congenital disorder involving deletion of chromosome 11q, detected by noninvasive prenatal testing at 14 weeks of gestation and confirmed on neonatal testing with array chromosomal genomic hybridization.
CONCLUSION: Noninvasive prenatal testing should be considered when multiple fetal anomalies are present and invasive testing is declined. As the clinical application of noninvasive prenatal testing continues to evolve, additional submicroscopic chromosomal information may be clinically helpful and should be confirmed with diagnostic testing until larger studies help further define the screening characteristics of noninvasive prenatal testing.

Entities:  

Mesh:

Year:  2015        PMID: 25569015     DOI: 10.1097/AOG.0000000000000528

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  1 in total

1.  11q23 deletion syndrome (Jacobsen syndrome) with severe bleeding: a case report.

Authors:  Yuko Ichimiya; Yuka Wada; Shinji Kunishima; Keiko Tsukamoto; Rika Kosaki; Haruhiko Sago; Akira Ishiguro; Yushi Ito
Journal:  J Med Case Rep       Date:  2018-01-08
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.