Risk Factors for Adverse Outcome in Fetuses With Heterotaxy Syndrome and Congenital Heart Disease
Fuente:
Wiley Open Access
Guardado en:
| Autores principales: | Anita Szwast, Jill J. Savla, Chris Penney, Priya Sharma, Jack Rychik |
|---|---|
| Formato: | Artículo Open Access |
| Publicado: |
Wiley
2026
|
| Materias: | |
| Acceso en línea: | |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
Hydroxychloroquine After Complete Heart Block Diagnosis and Relationship to Patient Outcomes: A Descriptive Cohort Study
por: Elizabeth L. Carter, et al.
Publicado: (2025)
por: Elizabeth L. Carter, et al.
Publicado: (2025)
Selective Fetoscopic Laser Photocoagulation of Placental Anastomoses Leads to Early Reduction of Cardiovascular Burden in the Twin‐Twin Transfusion Syndrome
por: Kasey J. Chaszczewski, et al.
Publicado: (2025)
por: Kasey J. Chaszczewski, et al.
Publicado: (2025)
Placental and Fetal Brain Volumes in Congenital Heart Disease Are Smallest Among Fetuses With Genetic Abnormalities
por: Sonali Ajwani, et al.
Publicado: (2025)
por: Sonali Ajwani, et al.
Publicado: (2025)
Neurosonographic Evaluation of Cerebral Cortical Development in Fetuses With Congenital Heart Disease: A Systematic Review of the Literature
por: Marcelo Dantas Cerqueira Monteiro, et al.
Publicado: (2025)
por: Marcelo Dantas Cerqueira Monteiro, et al.
Publicado: (2025)
mRNA Expression to Assess Hypoxia and Angiogenesis in Decidual Tissue of Term Fetuses With a Congenital Heart Disease
por: Maartje C. Snoep, et al.
Publicado: (2025)
por: Maartje C. Snoep, et al.
Publicado: (2025)
Longitudinal Magnetic Resonance Imaging Study of Hemodynamic Changes in the Third Trimester in Fetuses With Major Congenital Heart Defects and Healthy Fetuses
por: Signe G. Hellmuth, et al.
Publicado: (2025)
por: Signe G. Hellmuth, et al.
Publicado: (2025)
Diffusion Tensor Imaging of Fetuses With Congenital Diaphragmatic Hernia
por: Usha D. Nagaraj, et al.
Publicado: (2025)
por: Usha D. Nagaraj, et al.
Publicado: (2025)
Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
por: Yan Lü, et al.
Publicado: (2024)
por: Yan Lü, et al.
Publicado: (2024)
Prenatal and Perinatal Outcomes in Fetuses With Macrocystic Congenital Pulmonary Airway Malformations: Thoracoamniotic Shunting Versus Expectant Management
por: Laurence Sophie Carmant, et al.
Publicado: (2026)
por: Laurence Sophie Carmant, et al.
Publicado: (2026)
Can Fetal Heterotaxy Syndrome Be Diagnosed Through Prenatal Ultrasound in the First Trimester (GA 11+0−13+6 Weeks)?
por: Biying Huang, et al.
Publicado: (2025)
por: Biying Huang, et al.
Publicado: (2025)
Is there an increased risk of genetic abnormalities in fetuses with congenital heart disease in the setting of growth restriction?
por: Kathleen Gianforcaro, et al.
Publicado: (2024)
por: Kathleen Gianforcaro, et al.
Publicado: (2024)
Prenatal Diagnosis of Congenital Heart Disease in a Developing Country—A Cross‐Sectional Study
por: Lina Hammoud, et al.
Publicado: (2026)
por: Lina Hammoud, et al.
Publicado: (2026)
Maternal Vascular Malperfusion and Anatomic Cord Abnormalities Are Prevalent in Pregnancies With Fetal Congenital Heart Disease
por: Chrystalle Katte Carreon, et al.
Publicado: (2024)
por: Chrystalle Katte Carreon, et al.
Publicado: (2024)
Fetal Diagnosis of Hypoplastic Left Heart Syndrome With Restrictive Atrial Septum—Atrial Septal Morphology, Associated Lung Disease and Outcomes
por: Sofie Dannesbo, et al.
Publicado: (2025)
por: Sofie Dannesbo, et al.
Publicado: (2025)
Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2
por: Natalie Burrill, et al.
Publicado: (2024)
por: Natalie Burrill, et al.
Publicado: (2024)
Intrauterine Transfusions in Fetuses Affected by Parvovirus B19: Complications, Challenges and Outcomes
por: Banu Özbakir, et al.
Publicado: (2026)
por: Banu Özbakir, et al.
Publicado: (2026)
Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
por: Brian Burnett, et al.
Publicado: (2024)
por: Brian Burnett, et al.
Publicado: (2024)
A Whole MED12 Gene Deletion in a Female Fetus With Features Encountered in Hardikar Syndrome
por: Liping Wu, et al.
Publicado: (2024)
por: Liping Wu, et al.
Publicado: (2024)
Pregnancy Complications in Fetal Congenital Heart Disease: A Result of Common Early Developmental Pathways Rather Than Fetal Hemodynamics
por: Maartje C. Snoep, et al.
Publicado: (2025)
por: Maartje C. Snoep, et al.
Publicado: (2025)
Fetal Speckle Tracking Echocardiography Measured Global Longitudinal Strain and Strain Rate in Congenital Heart Disease: A Systematic Review and Meta‐Analysis
por: Sarah van den Wildenberg, et al.
Publicado: (2024)
por: Sarah van den Wildenberg, et al.
Publicado: (2024)
Theoretical Performance of Comprehensive Non‐Invasive Prenatal Screening in Congenital Heart Defects
por: Emily Yang, et al.
Publicado: (2026)
por: Emily Yang, et al.
Publicado: (2026)
Fetal Sylvian Fissure Maturation in Congenital Heart Disease and Its Relation to Expected Brain Arterial Oxygen Saturation: A Longitudinal Study
por: Xiaowei Xiong, et al.
Publicado: (2026)
por: Xiaowei Xiong, et al.
Publicado: (2026)
Associations of Physician Perspectives, Personal Choices, and Counseling for Severe Congenital Heart Defects
por: Joyce L. Woo, et al.
Publicado: (2025)
por: Joyce L. Woo, et al.
Publicado: (2025)
Observed/Expected Lung‐To‐Head Ratio and Total Lung Volumes That Identify Fetuses With Severe Congenital Diaphragmatic Hernia in a North American Fetal Center
por: Juliana Gebb, et al.
Publicado: (2025)
por: Juliana Gebb, et al.
Publicado: (2025)
Video Clip Extraction From Fetal Ultrasound Scans Using Artificial Intelligence to Allow Remote Second Expert Review for Congenital Heart Disease
por: Thomas G. Day, et al.
Publicado: (2025)
por: Thomas G. Day, et al.
Publicado: (2025)
Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin–Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features
por: Rachel A. Veazey, et al.
Publicado: (2024)
por: Rachel A. Veazey, et al.
Publicado: (2024)
Assessment of Fetal Cardiac Geometry and Systolic Function in Fetuses With Ventricular Septal Defect During the Second Trimester Using Fetal Heart Quantification Technology
por: Li Hou, et al.
Publicado: (2025)
por: Li Hou, et al.
Publicado: (2025)
Experimental Impact of Increasing Circuit Resistance in the Artificial Womb
por: Haiyan Cao, et al.
Publicado: (2025)
por: Haiyan Cao, et al.
Publicado: (2025)
Novel Fetal Phenotype for Pan‐Chung‐Bellen Syndrome Including Congenital Diaphragmatic Hernia
por: Nimerta Sandhu, et al.
Publicado: (2025)
por: Nimerta Sandhu, et al.
Publicado: (2025)
Congenital Vascular Anomalies: Prenatal Diagnosis, Perinatal Outcome and Postnatal Follow up
por: Stefano Faiola, et al.
Publicado: (2025)
por: Stefano Faiola, et al.
Publicado: (2025)
Navigating the Challenges of Exome Sequencing in Structurally Normal Fetuses
por: Sylvie Langlois, et al.
Publicado: (2025)
por: Sylvie Langlois, et al.
Publicado: (2025)
The Challenges of Performing Exome Sequencing in Structurally Normal Fetuses
por: Natalie Chandler, et al.
Publicado: (2024)
por: Natalie Chandler, et al.
Publicado: (2024)
Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney
por: Qiu‐Xia Yu, et al.
Publicado: (2026)
por: Qiu‐Xia Yu, et al.
Publicado: (2026)
Whole Exome Sequencing in a Population of Fetuses With Structural Anomalies
por: Natalie Burrill, et al.
Publicado: (2025)
por: Natalie Burrill, et al.
Publicado: (2025)
Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
por: Yiyun Xu, et al.
Publicado: (2025)
por: Yiyun Xu, et al.
Publicado: (2025)
Management and Outcomes in Isolated Congenital Aqueductal Stenosis: A Single‐Center Retrospective Cohort Study
por: Enaja V. Sambatur, et al.
Publicado: (2025)
por: Enaja V. Sambatur, et al.
Publicado: (2025)
Middle Cerebral Artery Peak Systolic Velocity in Fetuses With Transposition of the Great Arteries
por: Ditte S. Jørgensen, et al.
Publicado: (2025)
por: Ditte S. Jørgensen, et al.
Publicado: (2025)
Chromosomal Aberrations in Fetuses With Isolated Persistent Right Umbilical Vein—A Nationwide Study
por: Cathrine Vedel, et al.
Publicado: (2025)
por: Cathrine Vedel, et al.
Publicado: (2025)
Clinical and Molecular Features of Ciliopathies Diagnosed by Prenatal Exome Sequencing in Fetuses With Ultrasound Abnormalities
por: Xiaofan Zhu, et al.
Publicado: (2025)
por: Xiaofan Zhu, et al.
Publicado: (2025)
Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene
por: Cordelia R. Muir, et al.
Publicado: (2025)
por: Cordelia R. Muir, et al.
Publicado: (2025)
Ejemplares similares
-
Hydroxychloroquine After Complete Heart Block Diagnosis and Relationship to Patient Outcomes: A Descriptive Cohort Study
por: Elizabeth L. Carter, et al.
Publicado: (2025) -
Selective Fetoscopic Laser Photocoagulation of Placental Anastomoses Leads to Early Reduction of Cardiovascular Burden in the Twin‐Twin Transfusion Syndrome
por: Kasey J. Chaszczewski, et al.
Publicado: (2025) -
Placental and Fetal Brain Volumes in Congenital Heart Disease Are Smallest Among Fetuses With Genetic Abnormalities
por: Sonali Ajwani, et al.
Publicado: (2025) -
Neurosonographic Evaluation of Cerebral Cortical Development in Fetuses With Congenital Heart Disease: A Systematic Review of the Literature
por: Marcelo Dantas Cerqueira Monteiro, et al.
Publicado: (2025) -
mRNA Expression to Assess Hypoxia and Angiogenesis in Decidual Tissue of Term Fetuses With a Congenital Heart Disease
por: Maartje C. Snoep, et al.
Publicado: (2025)