Buchumschlag

Has the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?

Fuente: Wiley Open Access

Gespeichert in:

Bibliographische Detailangaben
Hauptverfasser:	Line Raaby, Stina Lou, Rikke Ramløv Lodberg Ivarsen, Jette Sørensen, Ole Halfdan Larsen, Ida Vogel
Format:	Artículo Open Access
Veröffentlicht:	Wiley 2024
Schlagworte:	Prenatal Diagnosis
Online-Zugang:	Acceder al recurso
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge

Use of cell‐free non‐invasive prenatal testing in pregnancies affected by placental mosaicism
von: Ida Charlotte Bay Lund, et al.
Veröffentlicht: (2024)

Is there an increased risk of genetic abnormalities in fetuses with congenital heart disease in the setting of growth restriction?
von: Kathleen Gianforcaro, et al.
Veröffentlicht: (2024)

Performance of cell‐free DNA testing for common fetal trisomies in triplet pregnancies
von: Hoda Zakaria, et al.
Veröffentlicht: (2024)

The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta‐analysis
von: K. Reilly, et al.
Veröffentlicht: (2024)

Prenatal detection rates for congenital heart disease using abnormal obstetrical screening ultrasound alone as indication for fetal echocardiography
von: Sanjay Vepa, et al.
Veröffentlicht: (2024)

Prenatal diagnosis of ROR‐2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities
von: Liying Yang, et al.
Veröffentlicht: (2024)

Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare
von: Ida Vogel, et al.
Veröffentlicht: (2025)

Deep‐learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy
von: Bhavya Kasera, et al.
Veröffentlicht: (2024)

High positive predictive value 22q11.2 microdeletion screening by prenatal cell‐free DNA testing that incorporates fetal fraction amplification
von: Carly Hammer, et al.
Veröffentlicht: (2024)

Management of fetal head and neck masses: Evaluation of prenatal factors associated with airway obstruction and decision for definitive airway and ex‐utero intrapartum treatment at birth
von: Nicholas Schmoke, et al.
Veröffentlicht: (2024)

Perspectives of pregnant women on broadening the scope of noninvasive prenatal testing from screening for foetal aneuploidies to prediction of adverse pregnancy outcomes: A qualitative study
von: Ellis C. Becking, et al.
Veröffentlicht: (2024)

Proposal for standardized prenatal assessment of fetal open dysraphisms by the European reference network for Intellectual disability, TeleHealth, Autism and Congenital Anomalies (ITHACA) and eUROGEN
von: Lucie Guilbaud, et al.
Veröffentlicht: (2024)

Associations and outcomes of prenatally detected rhombencephalosynapsis
von: Yada Kunpalin, et al.
Veröffentlicht: (2024)

Telegenetics to provide comprehensive prenatal diagnosis
von: April D. Adams, et al.
Veröffentlicht: (2024)

Improving prenatal diagnosis through standards and aggregation
von: Michael H. Duyzend, et al.
Veröffentlicht: (2024)

The bright future of fetal cardiology
von: Lindsay R. Freud, et al.
Veröffentlicht: (2024)

Has the Era of Individualized Intrauterine Treatment for Congenital Adrenal Hyperplasia Arrived?
von: Xinyu Fu, et al.
Veröffentlicht: (2025)

Interdependence of placenta and fetal cardiac development
von: Rachel L. Leon, et al.
Veröffentlicht: (2024)

Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders
von: Christel Thauvin‐Robinet, et al.
Veröffentlicht: (2024)

Case report of fetus with Lowe syndrome: Expanding the prenatal phenotype
von: Natalie Burrill, et al.
Veröffentlicht: (2024)

Fetal bradycardia in open versus fetoscopic prenatal repair of spina bifida
von: Steven T. Papastefan, et al.
Veröffentlicht: (2024)

Patient experiences with prenatal cell‐free DNA screening in a safety net setting
von: Kirsten A. Riggan, et al.
Veröffentlicht: (2024)

Considerations for specialized maternal–fetal care in the Somali‐American community
von: Stephanie A. Eyerly‐Webb, et al.
Veröffentlicht: (2024)

Inconsistencies between prenatal diagnostic and genetic testing laboratories on variant validation of rare monogenic diseases
von: Liling Lin, et al.
Veröffentlicht: (2024)

Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C
von: Courtney P. Verscaj, et al.
Veröffentlicht: (2024)

Transforming congenital heart disease management: Advances in fetal cardiac interventions
von: Stephanie Guseh, et al.
Veröffentlicht: (2024)

Structured reporting in fetal magnetic resonance imaging with congenital diaphragmatic hernia
von: G. Thater, et al.
Veröffentlicht: (2024)

Neighborhood deprivation is not associated with abortion consideration or completion in patients with fetal myelomeningocele
von: Steven T. Papastefan, et al.
Veröffentlicht: (2024)

Length of hysterotomy for fetal spina bifida repair is associated with prematurity risk
von: Kanokwaroon Watananirun, et al.
Veröffentlicht: (2024)

Knowledge gaps and confidence in counseling about aneuploidy screening and testing: A survey of prenatal care clinicians
von: M. M. Thorsen, et al.
Veröffentlicht: (2024)

Artificial intelligence‐based diagnosis in fetal pathology using external ear shapes
von: Quentin Hennocq, et al.
Veröffentlicht: (2024)

Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review
von: Vivien Cuvelier, et al.
Veröffentlicht: (2024)

Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males
von: Brighton Goodhue, et al.
Veröffentlicht: (2024)

Unbalanced X;Y translocations carrying SRY in prenatal settings: Clinical, molecular, and cytogenetic analysis of three cases
von: Xijing Liu, et al.
Veröffentlicht: (2024)

Association of right aortic arch and agenesis of ductus arteriosus in prenatal tetralogy of Fallot spectrum and its clinical implications
von: Adeline Walter, et al.
Veröffentlicht: (2024)

Women's attitudes towards disclosure of genetic information in pregnancy with varying levels of penetrance
von: Vitalia Libman, et al.
Veröffentlicht: (2024)

Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies
von: M. A. Lugthart, et al.
Veröffentlicht: (2024)

The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort study
von: Geerke M. Eggenhuizen, et al.
Veröffentlicht: (2024)

Response to the correspondence on “Performance of single‐gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting”
von: Julia Wynn, et al.
Veröffentlicht: (2024)

Pregnant women's informational needs prior to decisions about prenatal diagnosis for chromosomal anomalies—A Q methodological study
von: Ellen Ternby, et al.
Veröffentlicht: (2024)