Literature DB >> 16449179

Monozygotic twins discordant for monosomy 21 detected by first-trimester nuchal translucency screening.

Po-Jen Cheng1, Sheng-Wen Shaw, Jin-Chung Shih, Yung-Kuei Soong.   

Abstract

BACKGROUND: Chromosomal abnormality in one fetus of a monozygotic twin pregnancy is rare, and discussion of prenatal detection of such a case offers some insight into this clinical problem. CASE: A 28-year-old gravida 1 had ultrasound screening at 11 weeks of gestation that revealed a monochorionic, diamniotic twin pregnancy with increased nuchal translucency (7.7 mm) in one fetus. Subsequent evaluation showed one 45,XY,-21 karyotype and one normal male karyotype. The pregnancy was monozygous by DNA analysis. The affected neonate died 5 minutes after delivery of both twins by cesarean.
CONCLUSION: Monochorionic twins discordant for fetal abnormalities can be evaluated with molecular analysis. Study of such cases may reveal the extent to which an early diagnosis can lead to therapeutic interventions to support survival of the viable twin.

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Mesh:

Year:  2006        PMID: 16449179     DOI: 10.1097/00006250-200602001-00041

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


  5 in total

1.  Monozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report.

Authors:  Gabriela Tauwinklova; Renata Gaillyova; Pavel Travnik; Eva Oracova; Katerina Vesela; Lenka Hromadova; Jan Vesely; Petra Musilova; Jiri Rubes; Jitka Kadlecova; Iva Slamova; Eva Makaturova; Vladimira Vranova
Journal:  J Assist Reprod Genet       Date:  2010-08-11       Impact factor: 3.412

Review 2.  Constitutional and acquired autosomal aneuploidy.

Authors:  Colleen Jackson-Cook
Journal:  Clin Lab Med       Date:  2011-12       Impact factor: 1.935

Review 3.  Screening and Invasive Testing in Twins.

Authors:  Giovanni Monni; Ambra Iuculano; Maria Angelica Zoppi
Journal:  J Clin Med       Date:  2014-07-29       Impact factor: 4.241

4.  Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development.

Authors:  Cathrine Jespersgaard; Ida N Damgaard; Nanna Cornelius; Iben Bache; Niels Knabe; Maria J Miranda; Zeynep Tümer
Journal:  Mol Cytogenet       Date:  2016-02-04       Impact factor: 2.009

5.  Diagnosis of chromosomal abnormalities in a patient with thanatophoric dysplasia (TD) type I: The first report describing an important association between cytogenetic findings and TD.

Authors:  Mehmet Turgut; Osman Demirhan; Erdal Tunc; Ibrahim Hakan Bucak; Perihan Yasemen Canoz; Fatih Temiz; Gokhan Tumgor
Journal:  Am J Case Rep       Date:  2012-06-13
  5 in total

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