647 posters, 18 topics, 19 sessions, 2,121 authors, 360 institutions
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35th ISUOG World Congress on Ultrasound in Obstetrics and Gynecology
September 14 - 17, 2025 | Cancún, Mexico
Posters by Session
EP11.24
Decision-making after chorionic villus sampling (CVS): factors associated with pregnancy termination or continuation
D. A. Febres-Cordero, R. Germano Toledo, J. Agudogo, A. Macharia, A. Modest, B. O'Brien, Y. Oyelese
Beth Israel Deaconess Medical Center
Poster Presenter: Daniela Febres-Cordero
EP11.25
A unique case of prenatal diagnosis of vascular Ehlers-Danlos syndrome
E. Bertucci, S. Ceffa, F. G. Sileo, G. Sartor, A. La Marca, M. Gnazzo, A. Novelli
Modena and Reggio Emilia University, Universita degli Studi di Modena e Reggio Emilia
Poster Presenter: Emma Bertucci
EP11.26
Survey of perception of the state of the ultrasound screening at 11-14 weeks in Colombia
A. Camacho, M. gamez posada, H. abril huertas, D. parra vernaza, V. riaño piña
Universidad Antonio Narino Facultad de Medicina, Clinica De La Mujer
Poster Presenter: Andres Camacho
EP11.27
Evaluation of the activity of a referral prenatal diagnosis center in Tunisia: a prospective multicenter study
A. Ghanem, H. Ben Ahmed, A. Masmoudi, D. Chelli
Centre de Maternite et de Neonatologie, Centre de Maternite et de Neonatologie
Poster Presenter: Ahmed Ghanem
EP11.28
Prenatal diagnosis of tuberous sclerosis
M. D. BULUS, P. T. Castro, C. Hygino, T. Fazecas, A. P. Matos, P. Daltro, E. Araujo Junior, H. Werner
Biodesign Lab Dasa/PUC-Rio, Biodesign Lab Dasa/PUC-Rio, Universidade Federal do Rio de Janeiro, Biodesing Lab PUC/DASA Rio de Janeiro, CDPI
Poster Presenter: Heron Werner
EP11.31
Hereditary xerocytosis in pregnancy: a case report
L. Alrahmani
Loyola University Chicago
Poster Presenter: Layan Alrahmani
EP11.32
Meckel-Gruber syndrome
L. Castañeda Cuba, D. L. Benites Revilla
Hospital Belen De Trujillo, Universidad Privada Antenor Orrego Facultad de Medicina Humana
Poster Presenter: Luis Enrique Castañeda Cuba
EP11.36
Non-immune hydrops fetalis with underlying AARS2 gene mutation with combined oxidative phosphorylation deficiency8: case report and literatures review
O. K. Alraqadi, T. Markova
Oman Medical Speciality Board
Poster Presenter: Omimah Alraqadi
EP11.37
Prenatal signs of cartilage hair hypoplasia overlapping phenotype with omenn syndrome
E. Bertucci, G. Galeati, M. Benuzzi, F. G. Sileo, C. Rossi, C. Fiorentini, A. Soresina, F. Porta, A. Insalaco, L. Lugli
Modena and Reggio Emilia University, Universita degli Studi di Modena e Reggio Emilia
Poster Presenter: Emma Bertucci