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Fetal Screening Panel for Chromosomal Abnormalities (Serum/Plasma)

Published: August 9, 2026Updated: August 16, 2026

This test measures specific substances in your blood to help assess the risk of certain chromosomal abnormalities in your baby.

Quick summary

["A simple blood test to check for genetic risks during pregnancy."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
50580-0
Short code
Mat scn for fetal abnormalities SerPl
Synonyms
Mat scn for fetal abnormalities SerPl
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
CPT
86430
Specimen volume
5 mL
Stability
Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
4–24 hours
Order
routine

What Does This Test Measure?

The test detects elevated levels of substances like **human chorionic gonadotropin (hCG)**, **non-protein-bound estriol (uE3)**, and **inhibin A**, which can indicate higher chances of conditions like Down syndrome, Edwards syndrome, or Patau syndrome. It also includes **PAPP-A (placental protein A)**, a protein produced by the placenta.

Why Might You Need This Test?

Your healthcare provider may recommend this test if you’re at higher risk for chromosomal abnormalities, such as having had a previous pregnancy affected by such conditions, being over 35 years old, or having certain genetic factors.

How Is the Test Performed?

A small blood sample is taken from your arm. The sample is sent to a lab where it’s analyzed using advanced techniques to measure the substances mentioned above.

What Are the Next Steps?

If the results suggest an increased risk, further diagnostic testing (such as amniocentesis or chorionic villus sampling) may be recommended to get more detailed information about your baby’s health.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical Significance: This test is primarily used as a **first-trimester screening** to identify potential risks of chromosomal abnormalities. While it doesn’t diagnose the condition, it helps guide decisions about additional testing. False positives or negatives can occur, so results should always be reviewed by a healthcare provider.

Short name

Fetal Chromosomal Screening Panel

Frequently asked questions

What does a positive result mean?
A positive or elevated result indicates an increased likelihood of chromosomal abnormalities, but it doesn’t confirm them. Your doctor will discuss next steps, such as further testing or monitoring.
How soon will I get my results?
Results are typically available within 1–2 weeks after the blood draw. Your healthcare provider will explain the meaning of your results and any follow-up actions needed.
Can I eat or drink before this test?
No special preparation is needed. You can eat, drink, and take your usual medications as usual. Avoiding alcohol or caffeine before the test isn’t required unless instructed by your provider.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy