Characteristics and outcome of fetal nuchal translucency above 3.5 mm in the fi rst trimester

<p><strong>Objective</strong>: To describe the natural history of fetuses with a nuchal translucency (NT) above 3.5 mm when crown-rump length measures between 45 and 84 mm.</p><p><strong>Methods</strong>: We performed a retrospective cohort study of fetuses...

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Main Authors: Cátia Lourenço (Author), Inês Gouveia (Author), Ana Carriço (Author), Francisco Valente (Author)
Format: Book
Published: Open Journal of Biological Sciences - Peertechz Publications, 2019-07-22.
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LEADER 00000 am a22000003u 4500
001 peertech__10_17352_ojbs_000013
042 |a dc 
100 1 0 |a Cátia Lourenço  |e author 
700 1 0 |a  Inês Gouveia  |e author 
700 1 0 |a  Ana Carriço  |e author 
700 1 0 |a Francisco Valente  |e author 
245 0 0 |a Characteristics and outcome of fetal nuchal translucency above 3.5 mm in the fi rst trimester 
260 |b Open Journal of Biological Sciences - Peertechz Publications,   |c 2019-07-22. 
520 |a <p><strong>Objective</strong>: To describe the natural history of fetuses with a nuchal translucency (NT) above 3.5 mm when crown-rump length measures between 45 and 84 mm.</p><p><strong>Methods</strong>: We performed a retrospective cohort study of fetuses with fi rst trimester NT above 3.5 mm between January 2013 and March 2017.</p><p><strong>Results</strong>: A total of 75 cases with NT above 3.5 mm in the fi rst trimester were identifi ed. 3 cases were excluded (lost to follow-up), so that 72 cases were included. There were additional fi rst trimester markers of aneuploidy in 16 cases and 5 cases of major structural abnormalities diagnosed in the fi rst trimester ultrasound. 2 cases declined invasive testing. The karyotype was abnormal in 30 cases (43%), including 17 cases of trisomy 21. There were 25 terminations of pregnancy (34.7%), 11 fetal deaths (15.3%) and 36 livebirths (50%). The 36 live-born infants were followed. In this group 3 cases of trisomy 21, 1 case of unilateral hypoplasia of orbicularis oris, 1 Noonan-like syndrome, 1 case of 8p23.1 duplication (benign variant) and 1 case of lower limb lymphedema were observed.</p> 
540 |a Copyright © Cátia Lourenço et al. 
546 |a en 
655 7 |a Research Article  |2 local 
856 4 1 |u https://doi.org/10.17352/ojbs.000013  |z Connect to this object online.