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Prenatal imaging features and perinatal outcomes of foetal volvulus–A literature review
Prenatal imaging features and perinatal outcomes of foetal volvulus–A literature review
Abstract Objective To conduct a review of the literature on foetal volvulus with emphasis on prenatal imaging, pregnancy c...
PRENATAL DIAGNOSIS OF AICARDI SYNDROME BASED ON A SUGGESTIVE IMAGING PATTERN: A MULTICENTER CASE‐SERIES
PRENATAL DIAGNOSIS OF AICARDI SYNDROME BASED ON A SUGGESTIVE IMAGING PATTERN: A MULTICENTER CASE‐SERIES
ABSTRACTObjectivesTo characterize a suggestive prenatal imaging pattern of Aicardi syndrome using ultrasound and MRI.Metho...
Clinical outcomes of preimplantation genetic testing for hereditary cancer syndromes: A systematic review
Clinical outcomes of preimplantation genetic testing for hereditary cancer syndromes: A systematic review
Abstract The objective of this study was to review the published literature on clinical outcomes following preimplantation...
Non‐invasive prenatal testing detects blood chimerism in dizygotic twins
Non‐invasive prenatal testing detects blood chimerism in dizygotic twins
Key points What is already known? Placentas of dichorionic twins are fused in approximately 40% of the cases, and blood ch...
Trio exome sequencing is highly relevant in prenatal diagnostics
Trio exome sequencing is highly relevant in prenatal diagnostics
Abstract Objective About 3% of newborns show malformations, with about 20% of the affected having genetic causes. Clarific...
Factors impacting surgical decision making between prenatal and postnatal repair for myelomeningocele
Factors impacting surgical decision making between prenatal and postnatal repair for myelomeningocele
Abstract Objectives To determine factors influencing patients to choose prenatal or postnatal repair of their child's myel...
Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray
Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray
Abstract Objective To evaluate the pregnancy outcomes of fetuses with congenital heart disease (CHD) after chromosome micr...
High rate of abnormal findings in Prenatal Exome Trio in low risk pregnancies and apparently normal fetuses
High rate of abnormal findings in Prenatal Exome Trio in low risk pregnancies and apparently normal fetuses
Abstract Objective Data on the value of exome sequencing in fetuses with no structural anomalies are limited, especially i...
Prenatal work‐up, associated anomalies and postnatal outcomes of foetuses with 9–9.9 mm cerebral ventricular atria width
Prenatal work‐up, associated anomalies and postnatal outcomes of foetuses with 9–9.9 mm cerebral ventricular atria width
Abstract Objective To analyse prenatal work-up, associated anomalies and postnatal outcomes of foetuses with cerebral late...
A systematic review of maternal TORCH serology as a screen for suspected fetal infection
A systematic review of maternal TORCH serology as a screen for suspected fetal infection
Abstract Background The acronym ‘TORCH’ refers to well-recognised causes of perinatal infections: toxoplasmo...
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series
Abstract Objective Terminal 6q deletion is a rare genetic condition associated with a neurodevelopmental disorder characte...
Knowledge, attitudes, and practices of healthcare professionals working in prenatal diagnosis toward expanded non‐invasive prenatal testing in China
Knowledge, attitudes, and practices of healthcare professionals working in prenatal diagnosis toward expanded non‐invasive prenatal testing in China
Abstract Objectives To investigate the knowledge, attitudes, and practices of healthcare professionals (HCPs) working in p...
Prenatal phenotype of 47, XXY (Klinefelter syndrome)
Prenatal phenotype of 47, XXY (Klinefelter syndrome)
Abstract Objective There is a paucity of knowledge regarding the prenatal presentation of Klinefelter syndrome, or 47, XXY...
Severe fetal ventriculomegaly: Fetal morbidity and mortality, caesarean delivery rates and obstetrical challenges in a large prospective cohort
Severe fetal ventriculomegaly: Fetal morbidity and mortality, caesarean delivery rates and obstetrical challenges in a large prospective cohort
Abstract Introduction Severe fetal ventriculomegaly (VM) is defined as an enlargement of the atria of the lateral cerebral...
Triplet pregnancy: What do we tell the prospective parents
Triplet pregnancy: What do we tell the prospective parents
Abstract Experience managing triplet pregnancies has increased over the past few decades as the incidence has changed rela...
Perinatal outcome of twin‐to‐twin transfusion syndrome complicated with incidental septostomy after laser photocoagulation: A systematic review and meta‐analysis
Perinatal outcome of twin‐to‐twin transfusion syndrome complicated with incidental septostomy after laser photocoagulation: A systematic review and meta‐analysis
Abstract Aim To evaluate perinatal outcomes of incidental septostomy (IS) after laser photocoagulation for twin-to-twin tr...
Predicting fetal and neonatal demise after fetoscopy for twin–twin transfusion syndrome using recursive partitioning
Predicting fetal and neonatal demise after fetoscopy for twin–twin transfusion syndrome using recursive partitioning
Abstract Objective Donor demise after laser surgery for twin–twin transfusion syndrome (TTTS) is well-characterized...
Prediction of neonatal survival according to lung‐to‐head ratio in fetuses with right congenital diaphragmatic hernia (CDH): A multicentre study from the Latin American CDH Study Group registry
Prediction of neonatal survival according to lung‐to‐head ratio in fetuses with right congenital diaphragmatic hernia (CDH): A multicentre study from the Latin American CDH Study Group registry
Abstract Objective To evaluate survival outcomes of fetuses with right sided congenital diaphragmatic hernia (CDH) treated...
Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities
Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities
Abstract Backgrounds Microvillus inclusion disease (MVID) characterizes as intractable life-threatening watery diarrhea ma...
Utility of expanded carrier screening in pregnancies with ultrasound abnormalities
Utility of expanded carrier screening in pregnancies with ultrasound abnormalities
Abstract Objective Explore the utility of expanded carrier screening in evaluating heritable causes of congenital anomalie...
A novel “video‐game” simulator for training fetoscopic laser coagulation of anastomoses in twin‐to‐twin transfusion syndrome
A novel “video‐game” simulator for training fetoscopic laser coagulation of anastomoses in twin‐to‐twin transfusion syndrome
Key Points/Highlights   We have developed a high-fidelity interactive “video-game” simulator in order t...
Temporal persistence of residual fetal cell‐free DNA from a deceased cotwin after selective fetal reduction in dichorionic diamniotic twin pregnancies
Temporal persistence of residual fetal cell‐free DNA from a deceased cotwin after selective fetal reduction in dichorionic diamniotic twin pregnancies
Abstract Objectives To determine the temporal persistence of the residual cell-free DNA (cfDNA) of the deceased cotwin in ...
What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing
What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing
Abstract Objective To identify what online patient information (presented in English) is available to parents about prenat...
Outstanding clinical and research questions in complex twin and multiple pregnancy
Outstanding clinical and research questions in complex twin and multiple pregnancy
Corresponding Author Vascular Biology Research Centre, Molecular and Clinical S...
Complex multiple pregnancies: what's new?
Complex multiple pregnancies: what's new?
Early View EDITORIAL Tim Van Mieghem, Corresponding Author Division of...
Complex twins issue to Complex multiple pregnancies: what's new?
Complex twins issue to Complex multiple pregnancies: what's new?
Early View EDITORIAL Tim Van Mieghem, Corresponding Author Division of...
Open surgery for in utero repair of spina bifida: Microneurosurgery versus standard technique – A systematic review
Open surgery for in utero repair of spina bifida: Microneurosurgery versus standard technique – A systematic review
Abstract Background/objectives Prenatal myelomeningocele (MMC) repair has been shown to improve neurological outcomes. It ...
Perinatal outcomes after selective feticide via umbilical cord occlusion in complicated monochorionic pregnancies: A systematic review and meta‐analysis
Perinatal outcomes after selective feticide via umbilical cord occlusion in complicated monochorionic pregnancies: A systematic review and meta‐analysis
Abstract Objective We aimed to compare perinatal outcomes between umbilical cord occlusion techniques in monochorionic pre...
Editorial: complex twins issue
Editorial: complex twins issue
Abstract This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights r...
Trends in termination of pregnancy for neural tube defects in England and Wales from 2007 to 2017: Observational prospective study
Trends in termination of pregnancy for neural tube defects in England and Wales from 2007 to 2017: Observational prospective study
Abstract Background/Objective Neural tube defects (NTDs) affect approximately 300,000 pregnancies worldwide each year. Man...
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