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Your search keyword '"Bedei, Ivonne"' showing total 4 results
Start Over Author "Bedei, Ivonne" Publisher wiley
4 results on '"Bedei, Ivonne"'

2. Multicenter clinical experience with non‐invasive cell‐free DNA screening for monosomy X and related X‐chromosome variants

Author

Bedei, Ivonne, primary, Gehrke, Tascha, additional, Gloning, Karl‐Philipp, additional, Meyer‐Wittkopf, Matthias, additional, Willner, Daria, additional, Krapp, Martin, additional, Scharf, Alexander, additional, Degenhardt, Jan, additional, Heling, Kai‐Sven, additional, Kozlowski, Peter, additional, Trautmann, Kathrin, additional, Jahns, Kai M., additional, Geipel, Annegret, additional, Baumüller, Jan‐Erik, additional, Wilhelm, Lucas, additional, Gottschalk, Ingo, additional, Schröer, Andreas, additional, Graf, Alexander, additional, Wolter, Aline, additional, Schenk, Johanna, additional, Weber, Axel, additional, Van den Veyver, Ignatia B., additional, and Axt‐Fliedner, Roland, additional

Published
2023
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3. Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome

Author

Bedei, Ivonne, primary, Gloning, Karl‐Philipp, additional, Joyeux, Luc, additional, Meyer‐Wittkopf, Matthias, additional, Willner, Daria, additional, Krapp, Martin, additional, Scharf, Alexander, additional, Degenhardt, Jan, additional, Heling, Kai‐Sven, additional, Kozlowski, Peter, additional, Trautmann, Kathrin, additional, Jahns, Kai M., additional, Geipel, Annegret, additional, Tekesin, Ismail, additional, Elsässer, Michael, additional, Wilhelm, Lucas, additional, Gottschalk, Ingo, additional, Baumüller, Jan‐Erik, additional, Birdir, Cahit, additional, Schröer, Andreas, additional, Zöllner, Felix, additional, Wolter, Aline, additional, Schenk, Johanna, additional, Gehrke, Tascha, additional, Spaeth, Alicia, additional, and Axt‐Fliedner, Roland, additional

Published
2023
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4. Prenatal diagnosis and postnatal outcome of closed spinal dysraphism.

Author

Bedei I, Krispin E, Sanz Cortes M, Lombaard H, Zemet R, Whitehead WE, Belfort MA, and Huisman TAGM

Subjects
Pregnancy, Female, Infant, Newborn, Humans, Infant, Retrospective Studies, Prenatal Diagnosis methods, Magnetic Resonance Imaging methods, Ultrasonography, Prenatal methods, Arnold-Chiari Malformation, Spinal Dysraphism, Nervous System Malformations diagnosis
Abstract

Objective: To evaluate the prenatal diagnosis of closed dysraphism (CD) and its correlation with postnatal findings and neonatal adverse outcomes., Methods: A retrospective cohort study including pregnancies diagsnosed with fetal CD by prenatal ultrasound (US) and magnetic resonance imaging (MRI) at a single tertiary center between September 2011 and July 2021., Results: CD was diagnosed prenatally and confirmed postnatally in 12 fetuses. The mean gestational age of prenatal imaging was 24.2 weeks, in 17% the head circumference was ≤fifth percentile and in 25% the cerebellar diameter was ≤fifth percentile. US findings included banana sign in 17%, and lemon sign in 33%. On MRI, posterior fossa anomalies were seen in 33% of cases, with hindbrain herniation below the foramen magnum in two cases. Mean clivus-supraocciput angle (CSA) was 74°. Additional anomalies outside the CNS were observed in 50%. Abnormal foot position was demonstrated prenatally in 17%. Neurogenic bladder was present in 90% of patients after birth., Conclusion: Arnold Chiari II malformation and impaired motor function can be present on prenatal imaging of fetuses with CD and may be associated with a specific type of CD. Prenatal distinction of CD can be challenging. Associated extra CNS anomalies are frequent and the rate of neurogenic urinary tract dysfunction is high., (© 2023 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd.)

Published
2024
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