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The first-trimester screening is a set of prenatal tests conducted during the early stages of pregnancy, typically between weeks 11 and 14. This screening aims to assess the risk of certain chromosomal abnormalities and other congenital conditions in the developing fetus. The first-trimester screening typically involves a combination of ultrasound and blood tests, and it is often offered as part of routine prenatal care.
Here are the key components of the first-trimester screening:
An ultrasound is performed to measure the thickness of the nuchal translucency, which is the fluid-filled space at the back of the developing fetus's neck. An increased thickness may be associated with certain chromosomal abnormalities, such as Down syndrome.
A blood sample is taken from the pregnant woman to measure the levels of a protein called PAPP-A. Abnormal levels may be associated with an increased risk of chromosomal abnormalities.
Another blood sample is taken to measure the levels of human chorionic gonadotropin, a hormone produced during pregnancy. Deviations from expected levels may be associated with an increased risk of chromosomal abnormalities.
By combining the ultrasound measurements and blood test results, healthcare providers can calculate a more accurate assessment of the risk for conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).
It's important to note that the first-trimester screening provides a risk assessment, not a definitive diagnosis. If the screening indicates an increased risk, further diagnostic tests such as chorionic villus sampling (CVS) or amniocentesis may be offered for a more conclusive diagnosis.
The decision to undergo first-trimester screening or other prenatal tests is a personal one and may depend on various factors, including maternal age, medical history, and individual preferences. Expectant parents are encouraged to discuss their options and make informed decisions in consultation with their healthcare providers.