Imagen de Portada

Evolving Practices in Prenatal Open Spinal Dysraphism: A Global Survey of Selection Criteria, Surgical Techniques, and Diagnostic Trends

Fuente: Wiley Open Access

Guardado en:

Detalles Bibliográficos
Autores principales:	Corinna Keil, Noemi Wiora, Eyal Krispin, Anita Windhorst, Roland Axt‐Fliedner, Ivonne Bedei
Formato:	Artículo Open Access
Publicado:	Wiley 2025
Materias:	Prenatal Diagnosis
Acceso en línea:	Acceder al recurso
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares

Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal Cases
por: I. Bedei, et al.
Publicado: (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
por: Ivonne Bedei, et al.
Publicado: (2024)

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

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)

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

Mammalian target of rapamycin inhibitors: A new‐possible approach for in‐utero medication therapy
por: Shohra Qaderi, et al.
Publicado: (2024)

Diagnostic Yield After Postnatal Reanalysis of Prenatal Exome Sequencing Results
por: Kate Swanson, et al.
Publicado: (2025)

Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype
por: M. Codina‐Solà, et al.
Publicado: (2026)

Reporting Criteria for Prenatally Identified Variants of Uncertain Significance Differs Among Cytogenetics Laboratories in North America
por: Matthew A. Shear, et al.
Publicado: (2025)

Incidental Findings Identified by Prenatal Microarray Analysis and Consensus Reporting Criteria of the Catalan Public Health Network XIGENICS
por: Irene Mademont‐Soler, 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)

The Value of Enhancing Sonographic Phenotyping to Improve the Diagnostic Yield of Noninvasive Prenatal Diagnosis (NIPD) for Achondroplasia
por: Camille Verebi, et al.
Publicado: (2025)

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
por: Adesola C. Akinkuotu, et al.
Publicado: (2025)

Prenatal Ultrasound Features of Biliary Atresia: Diagnostic Significance of Abnormal Gallbladder Size and Hepatic Hilar Cyst
por: Wu Xu, et al.
Publicado: (2025)

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

Diagnostic Value of Cell‐Free DNA Fetal Fraction in Patients With Prenatally Suspected Placenta Accreta Spectrum Disorder
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)

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)

The Prenatal Neuro‐Radiological Phenotype Associated With a Recurrent Pathogenic Variant in PPP2R1A
por: Calder Hamill, et al.
Publicado: (2025)

The High Diagnostic Yield of Prenatal Exome Sequencing Followed by 3400 Gene Panel Analysis in 629 Ongoing Pregnancies With Ultrasound Anomalies
por: Karin E. M. Diderich, et al.
Publicado: (2024)

A Prospective Evaluation of the Diagnostic Utility for Low‐Coverage Genome Sequencing in Prenatal Samples: A Comparison With Chromosomal Microarray Analysis
por: Yan Yin, et al.
Publicado: (2025)

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

Prenatal Shwachman‐Diamond Syndrome: Diagnostic Challenges in Two Unrelated Cases With a Rare Clinical Presentation and Pseudogene Interference, and a Review of the Literature
por: Nathalie Vanden Eynde, 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)

Management and Outcomes in Isolated Congenital Aqueductal Stenosis: A Single‐Center Retrospective Cohort Study
por: Enaja V. Sambatur, et al.
Publicado: (2025)

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

High Risk for Rare Autosomal Trisomies Detected by Non‐Invasive Prenatal Testing: Prenatal Diagnosis and Pregnancy Outcomes
por: Zihan Jiang, et al.
Publicado: (2026)

Hemophilia A: An Ideal Disease for Prenatal Therapy
por: Christopher D. Porada, et al.
Publicado: (2025)

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

Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
por: Tony Lum, et al.
Publicado: (2026)

Brain Abnormalities in Prenatally Diagnosed Rubinstein‐Taybi Syndrome
por: Laurence S. Carmant, et al.
Publicado: (2025)

Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up
por: Alienor Jaillard, et al.
Publicado: (2024)

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

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

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

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

Prenatal Evaluation of Scrotal Masses: A Systematic Literature Review
por: Federica Romanzi, et al.
Publicado: (2025)

CUL3 ‐Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype
por: Yoel Gofin, et al.
Publicado: (2026)

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

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