Acetylcarnamnscnc
This test measures the level of acetylcarnitine, an important energy-related molecule, in the amniotic fluid surrounding the unborn baby.
{"Acetylcarnitine (C2) is measured in amniotic fluid to assess fetal metabolic health","The test helps screen for certain metabolic disorders that may affect the unborn baby","Sample is collected during amniocentesis procedure","Abnormal levels may indicate metabolic conditions requiring intervention","Results help doctors plan appropriate care during pregnancy and after birth"}
Key facts at a glance
- LOINC
- 50156-9
- Short code
- Acetylcarn Amn-sCnc
- Synonyms
- Acetylcarn Amn-sCnc
- Category
- chemistry
- Sample
- fluid
- Container
- Sterile tube
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Specimen volume
- 2-5 mL
- Stability
- Room temperature: 2h, Refrigerated: 24h
- Hemolysis max
- 300
- TAT
- 4–24 hours
- Order
- routine
What is this test?
The Acetylcarnitine (C2) test measures the amount of acetylcarnitine, a specialized molecule that helps transport fatty acids into cells for energy production, in the amniotic fluid. Amniotic fluid surrounds and protects the developing baby (fetus) in the womb. By measuring acetylcarnitine levels in this fluid, doctors can learn about the baby's metabolic status and detect potential metabolic disorders early in pregnancy.
How is the sample collected?
The sample is collected through a procedure called amniocentesis. During this procedure, a thin needle is inserted through the mother's abdomen into the uterus to withdraw a small amount of amniotic fluid. The procedure is typically performed under ultrasound guidance to ensure safety. Although amniocentesis carries a small risk of complications (such as infection or miscarriage), it is generally considered safe when performed by experienced healthcare providers.
Why is this test performed?
This test is primarily performed to screen for metabolic disorders in the fetus. Acetylcarnitine is a marker that can indicate how well the baby's body is processing fats and producing energy. Abnormal levels may suggest certain genetic metabolic conditions that affect how the body converts food into energy. Early detection allows healthcare providers to prepare for special care needs after birth and may influence treatment decisions during pregnancy.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Frequently asked questions
Is this test dangerous for my baby?
How long does it take to get results?
What do abnormal results mean?
Can this test predict all metabolic disorders?
Will I need to make decisions based on the results?
Sources
- 1
- 2
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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