RECURRENT INCREASED NUCHAL TRANSLUCENCY:
A FIRST TRIMESTER PRESENTATION OF
FAMILIAL 13p SATELLITE DELETION
Uzun I, Has R, Alici E, Ozdemir M, İnan C, Erzincan S
*Corresponding Author: Dr. Isil Uzun, Department of Obstetrics and Gynecology, Acibadem Hospital, Halit
Ziya Usakhıgil Street, Bakırkoy, İstanbul, Turkey. Tel: +90-212-414-4400. Fax: +90-212-414-4152. E-mail:
isiluzu@gmail.com
page: 103
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REFERENCES
1. Wyandt HE. Human Chromosome Variation:
Het-eromorphism and Polymorphism. New
York, NY, USA: Springer, 2011.
2. Nielsen J, Friederich U, Hreidarson AB. Frequency
of deletion of short arm satellites in acrocentric
chromosomes. J Med Genet. 1974; 11(2): 177-180.
3. Snijders RJ, Noble P, Sebire N, Souka A, Nicolaides
KH. UK Multicentre project on assessment
of risk of trisomy 21 by maternal age and
fetal nuchal-translucency thickness at 10-14
weeks of gestation. Fetal Medicine Foundation
First Trimester Screening Group. Lancet. 1998;
352(9125): 343-346.
4. Leung TY, Chan LW, Law LW, Sahota DS,
Fung TY, Lee TN, et al. First trimester combined
screening for trisomy 21 in Hong Kong:
Outcome of the first. J Matern Fetal Neonatal
Med. 2009; 22(4): 300-304.
5. Leung TY, Vogel I, Lau TK, Chong W, Hyett
JA, Peterson O. Identification of submicroscopic
chromosomal aberrations in fetuses with
increased nuchal translucency and apparently
normal karyotype. Ultrasound Obstet Gynecol.
2011; 38(3): 314-319.
6. Grande M, Jansen FA, Blumenfeld YJ, Fisher A,
Odibo AO, Haak MC, et al. Genomic microarray
in fetuses with increased nuchal translucency
and normal karyotype – A systematic review
and meta-analysis. Ultrasound Obstet Gynecol.
2015; 46(6): 650-658.
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