During the course, you will study the following key topics:

1. Prevalence of chromosomal abnormalities: You will learn about the frequency of various chromosomal abnormalities, enabling you to better understand and assess risks in patients.

2. Methodology for screening for chromosomal abnormalities: You will explore the details of ultrasound screening, including technical aspects and scanning protocols.

3. Assessment of specific syndromes: You will study the screening features of chromosomal abnormalities such as Patau syndrome, Edwards syndrome, Down syndrome, as well as additional markers such as cystic hygroma of the neck and others.

4. Assessment of nasal bones and tricuspid regurgitation: You will master methods for assessing the nasal bones and other markers that may be associated with the risk of chromosomal abnormalities, as well as understanding the significance of tricuspid regurgitation in the context of screening.

5. Assessment of blood flow and risks of chromosomal abnormalities: You will study the role of blood flow assessment in screening for chromosomal abnormalities and the methods for performing it.

6. Combined screening: You will become familiar with a combined approach to screening, incorporating ultrasound and biochemical methods, for more accurate determination of risks of chromosomal abnormalities.

This microcourse will provide you with all the necessary information and practical skills for effective screening and diagnosis of fetal chromosomal abnormalities. Expand your knowledge and improve the level of care for expectant mothers and their fetuses—register for the course right now!