Literature DB >> 21463211

Outcome of fetuses with Turner syndrome: a 10-year congenital anomaly register based study.

Narayan P Iyer1, David F Tucker, Selwyn H Roberts, Marsham Moselhi, Margery Morgan, Jean W Matthes.   

Abstract

OBJECTIVE: To describe the characteristics and outcome of fetuses with Turner syndrome reported to a national congenital anomalies register.
METHODS: All cases with a diagnosis of Turner syndrome reported to Congenital Anomaly Register and Information Service for Wales (CARIS) between 1 January 1998 and 31 December 2007 were included. The cases were grouped in five categories based on their outcomes: fetal loss (FL), termination of pregnancy (TOP), live birth (LB), and postnatal (PN) detection and comparison was undertaken between the groups.
RESULTS: One hundred twenty-four cases were reported during the study period. The prevalence of Turner syndrome was 1 in 4901 live female births. Seventy-four percent had 45 X karyotype while the rest had some form of Mosaic Turner karyotype. Pregnancy was terminated in 66% of antenatally diagnosed cases. FL and TOP groups had 92% and 87%, respectively, of 45 X karyotype - far greater than in the LB and PN groups. Increased nuchal thickness was the commonest anomaly noted in antenatal ultrasound and was a predictor for 45 X karyotype, FL, and termination.
CONCLUSION: Termination was the most common outcome of fetuses diagnosed antenatally with Turner syndrome. This has modified the natural history of Turner syndrome particularly in cases with Mosaic karyotype.

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Year:  2011        PMID: 21463211     DOI: 10.3109/14767058.2011.564688

Source DB:  PubMed          Journal:  J Matern Fetal Neonatal Med        ISSN: 1476-4954


  6 in total

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Authors:  Yi-Fei Li; Kai-Yu Zhou; Jie Fang; Chuan Wang; Yi-Min Hua; De-Zhi Mu
Journal:  World J Pediatr       Date:  2016-04-08       Impact factor: 2.764

2.  Turner syndrome - The clinical spectrum and management dilemmas.

Authors:  Krishanthy Thayalan; Kimberly Chung; Alka Kothari
Journal:  Australas J Ultrasound Med       Date:  2018-06-21

3.  Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2019-02-19

4.  Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features

Authors:  Nataliya Zelinska; Iryna Shevchenko; Evgenia Globa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2018-02-28

5.  Preliminary Evidence for Aortopathy and an X-Linked Parent-of-Origin Effect on Aortic Valve Malformation in a Mouse Model of Turner Syndrome.

Authors:  Robert B Hinton; Amy M Opoka; Obah A Ojarikre; Lawrence S Wilkinson; William Davies
Journal:  J Cardiovasc Dev Dis       Date:  2015-07-10

6.  EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies.

Authors:  Joan K Morris; Ester Garne; Maria Loane; Ingeborg Barisic; James Densem; Anna Latos-Bieleńska; Amanda Neville; Anna Pierini; Judith Rankin; Anke Rissmann; Hermien de Walle; Joachim Tan; Joanne Emma Given; Hugh Claridge
Journal:  BMJ Open       Date:  2021-06-28       Impact factor: 2.692

  6 in total

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