What is it about?
Submicroscopic chromosomal abnormalities should be accessed when the fetus was found to be with increased NT and normal karyotype. It is therefore important to inform parents in a professional prenatal counseling setting regarding the potential advantages of CMA.
Photo by Maria Teneva on Unsplash
Why is it important?
We recommend performing CMA to detect submicroscopic chromosomal abnormalities when the kayotype is normal, as the information derived can provide additional clinically relevant information .
Read the Original
This page is a summary of: Application of chromosomal microarray in fetuses with increased nuchal translucency, The Journal of Maternal-Fetal & Neonatal Medicine, January 2019, Taylor & Francis, DOI: 10.1080/14767058.2019.1569622.
You can read the full text:
The following have contributed to this page