Results 41 to 50 of about 5,907 (232)

Reappraising the Value of Fetal First-Trimester Ultrasonography

Maternal-Fetal Medicine, 2023
. In the last few years, the introduction of cell-free DNA has rapidly altered prenatal screening regimens and is increasingly offered as the second- or, at times, even the first-tier screening test.
Huirong Tang, Mingming Zheng, Yang Pan
doaj   +1 more source

A Practical Approach to Incorporating the Detailed First Trimester Ultrasound Examination into Clinical Practice

Journal of Ultrasound in Medicine, EarlyView.
Tremendous advances in ultrasound equipment and knowledge have expanded possibilities for the first trimester detailed ultrasound examination. Recommendations from national organizations to offer this service to patients with indications, coupled with recent modifications for dual use of the current procedural terminology code 76811 during pregnancy ...
Reem S Abu‐Rustum, Erica Smith, Kam Szlachetka, Oxana M Zarudskaya   +3 more
wiley   +1 more source

Predictive value of fetal nuchal translucency [PDF]

Medicinski Glasnik, 2011
Aim To determine the predictive value of fetal nuchal translucency(NT) measurements in the detection of chromosomopathy. Methods The investigation of NT included 317 pregnant women with singleton pregnancies of gestational age of 11 to 14 weeks with ...
Dragan Lončar
doaj  

The Clinical Significance of Fetal Intra‐Abdominal Umbilical Vein Varix A Comparative Study

Journal of Ultrasound in Medicine, EarlyView.
Objectives To clarify the clinical significance and optimal management of fetal intra‐abdominal umbilical vein varix (FIUVV). Methods A retrospective study comparing composite asphyxia‐related adverse outcomes including stillbirth, cesarean delivery due to non‐reassuring fetal heart rate (CD NRFHR), Apgar <7, Cord pH <7, neonatal intensive care unit ...
Keren Zloto, Ariella Wiener, Natalie Bibar, Raanan Meyer, Abeer Massarwa, Michal Fishel Bartal, Alina Weissmann‐Brenner, Eran Kassif, Tal Weissbach   +8 more
wiley   +1 more source

The Use of Ultrasound as a Potential Adjunct to Cell-Free Fetal DNA Screening for Aneuploidy at Weill Cornell Medical College, New York, USA

The Surgery Journal, 2018
Objective To evaluate the utility of ultrasound in identifying fetuses with uncommon chromosomal abnormalities that would be considered not detectable by cell-free fetal deoxyribonucleic acid (cfDNA).
Jessica Scholl, Stephen Chasen
doaj   +1 more source

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.
Yan Lü, Yi Yu, Jiazhen Chang, Mengmeng Li, Xueting Yang, Xiya Zhou, Na Hao, Hua Meng, Zhenghong Li, Lishuang Ma, Hui You, Shan Jian, Ying Wang, Shengjie Li, Yiqing Yu, Kaili Yin, Mingming Wang, Yulin Jiang, Qingwei Qi   +18 more
wiley   +1 more source

Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To describe the implementation of whole genome sequencing (WGS) in prenatal diagnostics and outline the national guideline system facilitating this. Methods Clinical guidelines for WGS in prenatal diagnostics were developed and implemented by the Danish Fetal Medicine Society.
Ida Vogel, Lotte Andreasen, Marie Balslev‐Harder, Naja Becher, Anja Ernst, Kasper Gadsbøll, Tina Duelund Hjortshøj, Marie Skov Hvidbjerg, Martin Larsen, Stina Lou, Ida Charlotte Bay Lund, Lars Henning Pedersen, Laura Kirstine Sønderberg Roos, Lene Sperling, Lone Sunde, Pernille Mathiesen Tørring, Cathrine Vedel, Olav Bjørn Petersen   +17 more
wiley   +1 more source

Ultrasound and echocardiographic findings obtained in the second and third trimesters of gestation in fetuses with normal karyotype and increased nuchal translucency

Journal of Ultrasonography, 2013
Introduction: Numerous papers have proven that an increased nuchal translucency is connected with a raised risk of chromosomal aberrations, but few analyses are related to the further state of fetuses with a normal karyotype.
Hanna Moczulska, Katarzyna Janiak, Maciej Słodki, Maria Respondek-Liberska   +3 more
doaj  

Antenatal Ultrasound Findings in Spinal Muscular Atrophy Type 0

Molecular Genetics & Genomic Medicine
Introduction Spinal muscular atrophy (SMA), caused by pathogenic variants in the survival motor neuron (SMN) gene, is the most common genetic cause of mortality in children under the age of two.
Stephanie Stokes, Madeline Snipes, Lee D. Moore, Natalia Schlabritz‐Lutsevich, Vidalin Amy, James Maher III   +5 more
doaj   +1 more source

Impact of nuchal cord on measurement of fetal nuchal translucency thickness [PDF]

Ultrasound in Obstetrics & Gynecology, 2007
AbstractObjectiveTo define the impact of nuchal cord on the measurement of fetal nuchal translucency thickness (NT).MethodsBetween December 2004 and June 2006, we examined prospectively 53 fetuses that were observed on routine first‐trimester ultrasound examination between 11 + 3 and 13 + 6 weeks of gestation to have nuchal cord causing an indentation ...
Matthias Scheier, I. Himmel, Daniel Egle, S. Viertl, Christian Marth, O. Huter, A Ramoni   +6 more
openaire   +3 more sources