If you’re at an increased risk of having a child with a chromosomal condition or a congenital anomaly, your healthcare provider may suggest a genetic test known as chorionic villus sampling (CVS). This first-trimester prenatal diagnostic procedure involves extracting a tiny tissue sample from the chorionic villi, which are the finger-like projections of the placenta. Since this sample carries the same genetic material as your developing baby, it can be utilized to screen for chromosomal disorders such as Down syndrome, as well as genetic diseases like cystic fibrosis and muscular dystrophy with a high level of precision. Additionally, CVS can reveal the sex of your baby, so be sure to communicate your preferences if you wish to keep that information private.
The results from a CVS test can significantly aid you, your partner, and your healthcare provider in planning for the future. They can guide your decisions regarding the continuation of the pregnancy, prepare you emotionally, and identify any necessary care or interventions for your baby post-birth.
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To summarize: Chorionic villus sampling is a critical test for expectant parents at higher risk for genetic conditions. This procedure not only aids in identifying potential health issues but also facilitates essential planning for the future, ensuring both you and your baby receive the best possible care and support.