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  2. 1016. α-fetoprotein (AFP) - prenatal diagnostics

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1016. α-fetoprotein (AFP) - prenatal diagnostics

1016. α-fetoprotein (AFP) - prenatal diagnostics

Turnaround time (days): 1

445 ₴

Important information

*For pregnant women at 14 -19 weeks of pregnancy inclusive.

Description

Alpha-fetoprotein (AFP) is a protein synthesized by the liver and gastrointestinal tract of the fetus. Its level in a pregnant woman's blood is a diagnostic marker for identifying the risk of congenital malformations, such as neural tube defects (anencephaly, spina bifida), anterior abdominal wall defects, and possible chromosomal abnormalities. AFP testing is often part of a triple or expanded biochemical screening during the second trimester. The test is recommended for all pregnant women between 15 and 20 weeks of gestation to promptly detect abnormalities and determine further pregnancy management.

Alpha-fetoprotein (AFP) is a glycoprotein produced by the yolk sac, liver, and intestinal epithelium of the fetus. During pregnancy, it performs functions similar to albumin: it transports nutrients, binds estrogens, regulates hormonal activity, and protects the fetus from the maternal immune system.

AFP levels in a pregnant woman's blood vary depending on gestational age. Its determination in the second trimester is an important diagnostic marker for detecting congenital malformations. Elevated levels may indicate neural tube defects, central nervous system anomalies, urinary tract pathologies, esophageal atresia, omphalocele, gastroschisis, or intrauterine liver necrosis.

Decreased AFP levels may be associated with chromosomal abnormalities, particularly trisomy 21 (Down syndrome). The test is recommended for routine prenatal screening in the second trimester of pregnancy, especially if suspicious changes are detected on ultrasound. AFP can be tested alone or as part of a triple test along with β-hCG and free estriol for a comprehensive assessment of the risk of chromosomal abnormalities.

When and who needs the test?

Pregnant women:

  • During the second trimester of pregnancy (14 weeks + 0 days – 19 weeks + 6 days), even with normal first-trimester screening results, to rule out congenital malformations.

As part of prenatal diagnosis, to detect:

  • neural tube defects (anencephaly, spina bifida), central nervous system anomalies, anterior abdominal wall defects (omphalocele, gastroschisis), esophageal and urinary tract atresia, and chromosomal abnormalities (trisomies, particularly trisomies 21).

As a standalone test or as part of triple screening in the second trimester.

Biological material

  • Venous blood

Preparing for a blood test

In order to exclude factors that may affect the test results, we recommend to follow the preparation rules:

  • an important condition for laboratory tests is to take blood on an empty stomach;
  • 6-12 hours before the test, you should avoid eating, drinking alcohol, smoking, and limit physical activity. Drinking...

Cheaper in a package

2060. Package #25 (Prenatal screening II trimester: AFP, β-HCG, E3)

Number of tests: 3
Free estriol (E3)
β-hCG total (human chorionic gonadotropin total) - prenatal
α-fetoprotein (AFP) - prenatal diagnostics

Turnaround time (days): 1

1150 ₴

1016. α-fetoprotein (AFP) - prenatal diagnostics

445 ₴

Information service

0 800 60 55 00

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