Supplement your learning for Ultrasound meets genetics.

Join us for this engaging and informative course. Together with a panel of expert speakers from around the world, they will dive into the latest discourse surrounding ultrasound in the assessment of pelvic floor disorder. This course offers attendees a valuable opportunity to gain a comprehensive understanding of the new advances in this area and learn how to apply them in practical situations.


Learning Objectives:

  • Learn how to link fetal anomalies with genetic diseases

  • Learn how to identify subtle ultrasound signs associated with genetic anomalies

  • Learn how to guide the type of genetic assessment when facing a structural anomaly

  • Learn how to integrate genetic and imaging to predict perinatal outcome and long-term prognosis

Explore the topic before you attend our course

In order to make the most of this learning experience and help you achieve your learning objectives, we have prepared a path to guide you from the essentials to our course’s topics through ISUOG resources. The material below, will take you from the most basics to a more comprehensive view of Ultrasound meets genetics, some open to everyone and some available only to ISUOG members –some may even grant you CME points:
Some of these activities are exclusively available to our members. Become a member today.

VISUOG

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Invasive Diagnostic Testing in Obstetrics: Amniocentesis and Chorionic Villus Sampling

Amniocentesis and chorionic villus sampling (CVS) are techniques in prenatal diagnostics, offering insights into fetal health, via assessment of analytes and genetics.

 

Patient Information

Ultrasound-Guided Procedures

This leaflet is to explain about ultrasound-guided procedures.

Amniocentesis

This leaflet is to help you understand Amniocentesis.

 

UOG Articles

Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta-analysis

A. Sotiriadis, E. Demertzidou, A. Ververi, E. Tsakmaki, C. Chatzakis, F. Mone

First published: 17 February 2025

 

Accuracy of cell-free fetal DNA in detecting chromosomal anomalies in women experiencing miscarriage: systematic review and meta-analysis

L. Della Valle, M. Piergianni, A. Khalil, G. Rizzo, I. Mappa, B. Matarrelli, A. Lucidi, L. Manzoli, M. E. Flacco, L. Stuppia, F. D'Antonio

First published: 07 December 2024

 

Influence of uterine fibroids on cell-free DNA screening: important but not definitive

Z.-Q. Xiao, D.-Z. Li

First published: 01 October 2024

 

Uterine fibroids and non-informative cell-free DNA screening results

D. L. Rolnik, Y. Raymond, T. Lee, J. Ramkrishna, F. da Silva Costa, M. Menezes, S. Meagher

First published: 23 August 2024

 

Pitfalls of systematic reviews and meta-analyses to assess the clinical utility of genomic investigations in prenatal diagnosis

F. Mone, D. L. Rolnik, A. Sotiriadis, R. J. Martinez-Portilla, A. Borrell

First published: 30 July 2024

 

Benefits of nuchal translucency measurement prior to 11–14 weeks' gestation

F. Jiang, D.-Z. Li

First published: 02 August 2024

 

Adverse pregnancy outcome in fetuses with early increased nuchal translucency: prospective cohort study

B. B. Bet, M. A. Lugthart, I. H. Linskens, M. C. van Maarle, E. van Leeuwen, E. Pajkrt

First published: 27 February 2024

 

Learning Modules

Optimising deep phenotyping through fetal imaging

K.Kagan 2024

Non-invasive prenatal testing is global consensus possible

K.Bilardo 2024

Stuart Campbell lecture: exome sequencing as a first- tier test for fetuses with severe central nervous system structural anomalies

Y.Yaron 2024

Equivocal and marginal indications for exome sequencing

A.Sotiriadis 2024

Knowledge sharing to ensure ultrasound and genetic testing complement each other in prenatal diagnosis

M.Norton, L.Dugoff 2023

The present and future of prenatal diagnosis way beyond chromosomal analysis

L.Chitty 2022

 

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