Cover Image

High Risk for Rare Autosomal Trisomies Detected by Non‐Invasive Prenatal Testing: Prenatal Diagnosis and Pregnancy Outcomes

Fuente: Wiley Open Access

Saved in:

Bibliographic Details
Main Authors:	Zihan Jiang, Wanjun Wang, Ying Zhang, Xiangyu Zhu, Wei Liu, Leilei Gu, Qiqi Xu, Yujie Zhu, Jie Li, Honglei Duan
Format:	Artículo Open Access
Published:	Wiley 2026
Subjects:	Prenatal Diagnosis
Online Access:	Acceder al recurso
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Confined Placental Mosaicism Detected With Non‐Invasive Prenatal Testing: Is There an Association Between Mosaic Ratio and Pregnancy Outcome?
by: Geerke M. Eggenhuizen, et al.
Published: (2024)

Maternal Mosaicism Challenges in Non‐Invasive Prenatal Diagnosis
by: Margot Comel, et al.
Published: (2025)

Prenatal Screening for Fetal X‐Linked Ichthyosis: A Large Cohort Study Combining Non‐Invasive Prenatal Testing and Maternal Serum Unconjugated Estriol Analysis
by: Miao Han, et al.
Published: (2026)

Application of Genetic Origin Analysis of Copy Number Variations in Non‐Invasive Prenatal Testing
by: Jing Wang, et al.
Published: (2024)

Prenatal Ultrasound in the Diagnosis of Anorectal Malformations: Correlating Prenatal Signs With Postnatal Outcomes
by: D. Huijgen, et al.
Published: (2024)

Sex Ratios at Birth Following Non‐Invasive Prenatal Testing in Victoria, Australia
by: Hilary Bowman‐Smart, et al.
Published: (2026)

Celocentesis for Prenatal Diagnosis of Rare Monogenic Diseases: Development, Validation, and Clinical Outcome on 876 Cases
by: Antonino Giambona, et al.
Published: (2026)

Clinical Implications of Low Cell‐Free DNA Fetal Fraction in Non‐Invasive Prenatal Testing: A Retrospective Cohort Study of 40,716 Pregnancies
by: Kayono Yamamoto, et al.
Published: (2025)

Non‐Invasive Prenatal Testing Results, Nuchal Translucency Size, and Second Trimester Resolution Modify First Trimester Cystic Hygroma Outcomes
by: Michelle Joy Wang, et al.
Published: (2025)

Theoretical Performance of Comprehensive Non‐Invasive Prenatal Screening in Congenital Heart Defects
by: Emily Yang, et al.
Published: (2026)

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
by: Connor Hartzell, et al.
Published: (2025)

Screening Positive for Rare Autosomal Aneuploidies Increases Frequency of Adverse Pregnancy Outcomes and Alters Clinical Management
by: Devika Chawla, et al.
Published: (2025)

Congenital Vascular Anomalies: Prenatal Diagnosis, Perinatal Outcome and Postnatal Follow up
by: Stefano Faiola, et al.
Published: (2025)

Prenatal Diagnosis of Caroli's Disease by Ultrasound and MRI Imaging
by: Ying‐Li Wei, et al.
Published: (2025)

Analysis of Prenatal Sonographic Features in Rare Fetal Giant Hepatic Hemangioma and Prediction of Prenatal Complications and Prognosis
by: Ling Xu, et al.
Published: (2025)

Blazing the Trail of Non‐Invasive Prenatal Screening Expanded Use: Healthcare Providers' Perspectives
by: Tierry M. Laforce, et al.
Published: (2025)

The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome‐SHS
by: Charlène Daval, et al.
Published: (2025)

Parental Somatic Mosaicism Detected During Prenatal Diagnosis
by: Natalie J. Chandler, et al.
Published: (2024)

PIGO Gene Variants: New Insights Into Prenatal Diagnosis
by: A. Zambiasi, et al.
Published: (2025)

Prenatal‐Onset Autosomal Dominant Polycystic Kidney Disease: Clinical Spectrum and Genetic Complexity of a Pseudo‐Recessive Phenotype
by: Margarita Sharova, et al.
Published: (2025)

Fetal Macrocephaly: Prenatal Findings and Follow‐Up in Cases With High Risk for Abnormal Outcome
by: Hadas Miremberg, et al.
Published: (2025)

Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non‐Isolated Clubfoot?
by: Jana M. de Vries, et al.
Published: (2025)

Response to the Correspondence by Jean‐Marie Jouannic et al. to: Prenatal Diagnosis and Postnatal Outcome of Closed Spinal Dysraphism. Prenat Diagn. 2024 Apr;44(4):499–510
by: Ivonne Bedei, et al.
Published: (2024)

The Importance of Clinical Acumen for Prenatal Diagnosis in an Increasingly Technological World
by: Teresa N. Sparks, et al.
Published: (2025)

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
by: Yiyun Xu, et al.
Published: (2025)

Prenatal Variable Expressivity of a Maternal FGFR1 Truncating Variant in Consecutive Pregnancies: A Dual‐Generation Case Report
by: Huining Jing, et al.
Published: (2026)

Prenatal Diagnostic Testing for Adult‐Onset Neurodegenerative Disease
by: Maya Rawal, et al.
Published: (2025)

Prenatal Diagnosis and Neurodevelopmental Outcome of Children With Marked Opening of the Fourth Ventricle: Challenges and Pitfalls in MRI Diagnostic Criteria
by: Léa Schieffer, et al.
Published: (2026)

Prenatal Diagnosis to Postnatal Outcomes of Saccular Forms of Closed Spina Dysraphism: A Single Center Retrospective Study
by: Yada Kunpalin, et al.
Published: (2025)

Vaginal Delivery in Cases of Prenatally Diagnosed Omphalocele: Feasibility and Outcomes
by: H. Heinrich, et al.
Published: (2025)

Prenatal Diagnosis of Shwachman–Diamond Syndrome: Fetal Compound Heterozygous Variants in the SBDS Gene Associated With Mildly Straight Ribs
by: Linyan Zhu, et al.
Published: (2025)

Prenatal Diagnosis of Horseshoe Lung: A Report of Three Cases and Review of the Literature
by: Benjamin Birene, et al.
Published: (2025)

Prenatal Diagnosis of Sotos Syndrome: Integrating Chromosomal Microarray Analysis and Exome Sequencing
by: Xi Yang, et al.
Published: (2025)

Perspectives on Fetal Sex and Prenatal Diagnosis of Differences of Sex Development Among Midwives
by: Madeline Dingle, et al.
Published: (2025)

Performance of Prenatal Cell‐Free DNA Screening for Foetal Chromosome Aneuploidies and Microdeletion/Microduplication Syndromes: A Retrospective Study of 64,482 Consecutive Cases From a Prenatal Diagnosis Centre in China
by: Feiyan Pan, et al.
Published: (2025)

Disparities in Prenatal Carrier Screening Including Partner Testing by Insurance Status
by: Spencer C. Darveau, et al.
Published: (2026)

Maternal Health Literacy and Prenatal Learning Experiences Related to Diagnosis and Surgical Management: A Qualitative Study of Women With Pregnancies Associated With Surgically Correctable Congenital Anomalies
by: Adesola C. Akinkuotu, et al.
Published: (2025)

Diagnostic Yield of Sequencing for Prenatal Diagnosis of Fetal Structural Anomalies: An Updated Systematic Review
by: Karen Mei Xian Lim, et al.
Published: (2026)

Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome
by: Mia B. Hodges, et al.
Published: (2025)

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder
by: Xiang‐Yi Jing, et al.
Published: (2025)