Fetal Pancreas in Growth Restriction: A Prenatal Window Into Metabolic and Genetic Risk
Fuente:
Wiley Open Access
Guardado en:
| Autores principales: | Hadas Miremberg, Catharina Bobrow, Noa Feldman, Noa Haggiag, Catherine Garel, Gustavo Malinger, Karina Krajden Haratz, Sharon Perlman |
|---|---|
| Formato: | Artículo Open Access |
| Publicado: |
Wiley
2025
|
| Materias: | |
| Acceso en línea: | |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly
por: Hadas Miremberg, et al.
Publicado: (2024)
por: Hadas Miremberg, et al.
Publicado: (2024)
Fetal Macrocephaly: Prenatal Findings and Follow‐Up in Cases With High Risk for Abnormal Outcome
por: Hadas Miremberg, et al.
Publicado: (2025)
por: Hadas Miremberg, et al.
Publicado: (2025)
Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly
por: Roee Birnbaum, et al.
Publicado: (2024)
por: Roee Birnbaum, et al.
Publicado: (2024)
Exome Sequencing in Prenatally Diagnosed Isolated Neural Tube Defects: A Subtype‐Specific Analysis
por: Adi Botvinik, et al.
Publicado: (2026)
por: Adi Botvinik, et al.
Publicado: (2026)
A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum
por: Karina Krajden Haratz, et al.
Publicado: (2024)
por: Karina Krajden Haratz, et al.
Publicado: (2024)
Severe Early‐Onset Fetal Growth Restriction: The Yield of Antenatal and Postnatal Genetic Testing
por: Matthew H. Mossayebi, et al.
Publicado: (2026)
por: Matthew H. Mossayebi, et al.
Publicado: (2026)
Fetal Anogenital Distance Correlates With Hypospadias and Curvature Severity
por: Michael Frumer, et al.
Publicado: (2025)
por: Michael Frumer, et al.
Publicado: (2025)
Prenatal Diagnosis of Arboleda‐Tham Syndrome Associated With KAT6A Variants Presented With Interrupted Inferior Vena Cava and Fetal Growth Restriction
por: Qiu‐Xia Yu, et al.
Publicado: (2025)
por: Qiu‐Xia Yu, et al.
Publicado: (2025)
Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra‐Cerebral Malformations
por: C. Kratochwila, et al.
Publicado: (2024)
por: C. Kratochwila, et al.
Publicado: (2024)
Prenatal Diagnosis of Horseshoe Lung: A Report of Three Cases and Review of the Literature
por: Benjamin Birene, et al.
Publicado: (2025)
por: Benjamin Birene, et al.
Publicado: (2025)
Perspectives on Fetal Sex and Prenatal Diagnosis of Differences of Sex Development Among Midwives
por: Madeline Dingle, et al.
Publicado: (2025)
por: Madeline Dingle, et al.
Publicado: (2025)
Moderate Diagnostic Yield of Exome Sequencing in Fetal Growth Restriction: Retrospective Insights
por: Maud Langeois, et al.
Publicado: (2026)
por: Maud Langeois, et al.
Publicado: (2026)
Cardiac Function in Fetal Growth Restriction: A Systematic Review and Meta‐Analysis
por: Alice D'Amico, et al.
Publicado: (2026)
por: Alice D'Amico, et al.
Publicado: (2026)
Hypospadias Associated With Fetal Growth Restriction: A Multicentric Descriptive and Prognostic Cohort Study
por: Manon Marquet, et al.
Publicado: (2024)
por: Manon Marquet, et al.
Publicado: (2024)
Perinatal Outcome of Early‐ and Late‐Onset Selective Fetal Growth Restriction in Monochorionic Diamniotic Twin Pregnancies
por: Li Zhao, et al.
Publicado: (2026)
por: Li Zhao, et al.
Publicado: (2026)
Middle Cerebral Artery Doppler and Cerebroplacental Ratio Predict Adverse Neurological Outcomes in Fetal Growth Restriction
por: Silvia Visentin, et al.
Publicado: (2026)
por: Silvia Visentin, et al.
Publicado: (2026)
Analysis of Prenatal Sonographic Features in Rare Fetal Giant Hepatic Hemangioma and Prediction of Prenatal Complications and Prognosis
por: Ling Xu, et al.
Publicado: (2025)
por: Ling Xu, et al.
Publicado: (2025)
Clinical Implications of Noninvasive Prenatal Testing Failures Due to Low Fetal Fraction: Associations With Adverse Maternal and Fetal Outcomes
por: Yuan Ren, et al.
Publicado: (2025)
por: Yuan Ren, et al.
Publicado: (2025)
Prenatal Detection of Fetal Abdominal Cysts: Can We Reassure Future Parents?
por: H. Heinrich, et al.
Publicado: (2026)
por: H. Heinrich, et al.
Publicado: (2026)
Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up
por: Alienor Jaillard, et al.
Publicado: (2024)
por: Alienor Jaillard, et al.
Publicado: (2024)
Can Prenatal Ultrasonographic Markers Predict Enteral Feeding Tolerance in Neonates With Fetal Omphalocele?
por: Maaike Hogerwerf, et al.
Publicado: (2025)
por: Maaike Hogerwerf, et al.
Publicado: (2025)
Diagnostic Yield of Sequencing for Prenatal Diagnosis of Fetal Structural Anomalies: An Updated Systematic Review
por: Karen Mei Xian Lim, et al.
Publicado: (2026)
por: Karen Mei Xian Lim, et al.
Publicado: (2026)
Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder
por: Xiang‐Yi Jing, et al.
Publicado: (2025)
por: Xiang‐Yi Jing, et al.
Publicado: (2025)
Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis
por: Maud Favier, et al.
Publicado: (2024)
por: Maud Favier, et al.
Publicado: (2024)
Prenatal Diagnosis and Neurodevelopmental Outcome of Children With Marked Opening of the Fourth Ventricle: Challenges and Pitfalls in MRI Diagnostic Criteria
por: Léa Schieffer, et al.
Publicado: (2026)
por: Léa Schieffer, et al.
Publicado: (2026)
Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort
por: Dana Brabbing‐Goldstein, et al.
Publicado: (2024)
por: Dana Brabbing‐Goldstein, et al.
Publicado: (2024)
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation
por: Elizabeth Goldmuntz, et al.
Publicado: (2024)
por: Elizabeth Goldmuntz, et al.
Publicado: (2024)
Cover Image
por: Noa Liscovitch‐Brauer, et al.
Publicado: (2024)
por: Noa Liscovitch‐Brauer, et al.
Publicado: (2024)
Prenatal Screening for Fetal X‐Linked Ichthyosis: A Large Cohort Study Combining Non‐Invasive Prenatal Testing and Maternal Serum Unconjugated Estriol Analysis
por: Miao Han, et al.
Publicado: (2026)
por: Miao Han, et al.
Publicado: (2026)
Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype
por: M. Codina‐Solà, et al.
Publicado: (2026)
por: M. Codina‐Solà, et al.
Publicado: (2026)
Diagnostic Value of Cell‐Free DNA Fetal Fraction in Patients With Prenatally Suspected Placenta Accreta Spectrum Disorder
por: Danielle Chirumbole, et al.
Publicado: (2025)
por: Danielle Chirumbole, et al.
Publicado: (2025)
The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies
por: Lisa S. Weingarten, et al.
Publicado: (2025)
por: Lisa S. Weingarten, et al.
Publicado: (2025)
Prenatal Diagnosed Agenesis of the Corpus Callosum: Identifying the Underlying Genetic Etiologies
por: Xing Wei, et al.
Publicado: (2024)
por: Xing Wei, et al.
Publicado: (2024)
Prenatal Diagnosis of Shwachman–Diamond Syndrome: Fetal Compound Heterozygous Variants in the SBDS Gene Associated With Mildly Straight Ribs
por: Linyan Zhu, et al.
Publicado: (2025)
por: Linyan Zhu, et al.
Publicado: (2025)
Perinatal Outcomes in Appropriately Grown Monochorionic Diamniotic Twins With Intermittent Absent and Reversed End‐Diastolic Umbilical Artery Flow Compared to Selective Fetal Growth Restriction Type III
por: Elizabeth Schlant, et al.
Publicado: (2024)
por: Elizabeth Schlant, et al.
Publicado: (2024)
Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non‐Isolated Clubfoot?
por: Jana M. de Vries, et al.
Publicado: (2025)
por: Jana M. de Vries, et al.
Publicado: (2025)
A Decade of Prenatal Genetic Diagnostics: Insights From 1949 Cases at a Medical Genetics Facility in South India
por: Roopadarshini Balasubramanian, et al.
Publicado: (2025)
por: Roopadarshini Balasubramanian, et al.
Publicado: (2025)
Integrating the Continuum of Genetic Testing From Fetus to Neonate: A Review of Prenatal Genetic Testing and the Overlap With Newborn Testing
por: Sarah Harris, et al.
Publicado: (2025)
por: Sarah Harris, et al.
Publicado: (2025)
The Role of Prenatal Ultrasound and Added Value of Post‐Mortem Radiographic Imaging With X‐Ray and CT in Suspected Fetal Skeletal Dysplasia
por: Katri Rajala, et al.
Publicado: (2024)
por: Katri Rajala, et al.
Publicado: (2024)
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)
Ejemplares similares
-
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly
por: Hadas Miremberg, et al.
Publicado: (2024) -
Fetal Macrocephaly: Prenatal Findings and Follow‐Up in Cases With High Risk for Abnormal Outcome
por: Hadas Miremberg, et al.
Publicado: (2025) -
Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly
por: Roee Birnbaum, et al.
Publicado: (2024) -
Exome Sequencing in Prenatally Diagnosed Isolated Neural Tube Defects: A Subtype‐Specific Analysis
por: Adi Botvinik, et al.
Publicado: (2026) -
A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum
por: Karina Krajden Haratz, et al.
Publicado: (2024)