Results 61 to 70 of about 11,570 (268)

Monoamniotic twins discordant for body stalk anomaly [PDF]

, 2015
Body stalk anomaly is a rare malformation. This anomaly in monozygotic twins is extremely unusual. We describe a case of monoamniotic pregnancy discordant for body stalk anomaly diagnosed at 11 weeks.
Domingues, AP, Fonseca, E, Moura, P, Tavares, M, Tavares, MV   +4 more
core   +1 more source

Deep Learning Measurement Model to Segment the Nuchal Translucency Region for the Early Identification of Down Syndrome [PDF]

, 2022
Mary Christeena Thomas, Sridhar P. Arjunan   +1 more
openalex   +1 more source

A Framework for Bioinformatic Reporting in Prenatal Sequencing: Insights From a Systematic Review

Prenatal Diagnosis, EarlyView.
ABSTRACT Genomic sequencing has become a key tool in the investigation of foetal anomalies, with a growing shift from targeted panels to exome and genome sequencing. These broader approaches generate significantly more data, underscoring the need for robust bioinformatics pipelines. However, practices vary widely between laboratories.
Ashley J. Pritchard, Karen Mei Xian Lim, Graeme Smith, Elizabeth Scotchman, Alexander Gibbs, Patrick Lombard, Natalie J. Chandler   +6 more
wiley   +1 more source

Fetal aorto-pulmonary window: case series and review of the literature [PDF]

, 2017
Aorto-pulmonary window is a rare congenital cardiac anomaly characterized by a communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare.
Carvalho, JS, Fotaki, A, Jicinska, H, Novaes, J   +3 more
core   +1 more source

Multiple pregnancy with complete hydatidiform mole and coexisting normal fetus: systematic review and meta‐analysis of clinical outcomes from non‐randomized studies

Ultrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective Complete hydatidiform mole and coexisting normal fetus (CHMCF) is a rare condition for which there is significant heterogeneity in diagnosis, counseling and management of complications. The objective of this study was to summarize the prevalence of clinical outcomes in reported cases of CHMCF.
N. Salmeri, A. Pizzetti, E. Grassi, R. Cioffi, G. Mangili, M. Seckl, A. Sotiriadis, M. Candiani, P. I. Cavoretto   +8 more
wiley   +1 more source

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

Prenatal ultrasound diagnosis and quality control of fetal nuchal translucency. [PDF]

Zhong Nan Da Xue Xue Bao Yi Xue Ban
Yuan X, Fu Y.
europepmc   +3 more sources

Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome [PDF]

, 2016
published_or_final_versio
Chan, KY, Kan, SYA, Kou, KOT, Kwok, SL, Leung, KY, Poon, CF, Tang, MHY   +6 more
core   +1 more source

The application of artificial intelligence in blind ultrasound sweep diagnostics for prenatal medicine: A systematic literature review

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
Artificial intelligence enables the interpretation of blind ultrasound sweeps for prenatal diagnostics. Applications include accurate gestational age estimation, amniotic fluid segmentation, fetal presentation classification, and placental localization.
Johanna Schott, Melanie Wilmes, Adeline Walter, Ruben Plöger, Ingo Gottschalk, Tanja Groten, Florian Recker   +6 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