Understanding Your Laboratory Test: What It Is, Why It Is Done, and What the Results Mean
This test measures a specific fatty acid metabolite in amniotic fluid to help detect certain metabolic disorders in the unborn baby.
{"Measures C14-OH acylcarnitine levels in amniotic fluid collected during pregnancy","Helps screen for fetal metabolic disorders affecting fatty acid breakdown","Results are interpreted along with other prenatal tests to assess baby's health","Abnormal results may require additional testing and genetic counseling","The test is part of prenatal metabolic screening, not routine pregnancy care"}
Key facts at a glance
- LOINC
- 50282-3
- Short code
- 3OH-Tdecanoylcarn Amn-sCnc
- Synonyms
- 3OH-Tdecanoylcarn 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
This test is a laboratory procedure in which a small sample of your blood, urine, or other body material is analyzed to measure specific substances, cells, or markers that show how your body is functioning and whether illness may be present.
The 3-Hydroxytetradecanoylcarnitine (C14-OH) test measures the amount of a specific fatty acid metabolite called C14-OH acylcarnitine in the amniotic fluid that surrounds the baby during pregnancy. Acylcarnitines are substances produced when the body breaks down fats for energy. This test uses a sample of amniotic fluid collected during amniocentesis, a procedure where a small amount of fluid is removed from the uterus for testing.
Your doctor may order this test as part of a routine health checkup, to investigate symptoms such as fatigue, pain, or fever, to help diagnose a medical condition, to monitor a chronic disease, or to track how well a treatment is working over time.
This test is performed to screen for certain metabolic disorders that a baby may have before birth. These disorders affect how the baby's body processes fats for energy. Detecting these conditions during pregnancy allows healthcare providers to prepare for special care the baby may need immediately after birth. The test is usually ordered when there is a family history of metabolic disorders or when other screening tests suggest a potential problem.
Your results are compared with normal reference ranges, and values within those ranges usually suggest typical body function. Out-of-range values may point to infection, inflammation, anemia, hormone imbalance, or another condition, but they do not provide a diagnosis by themselves. Your doctor will interpret the numbers along with your symptoms, medical history, and other test results, and will explain what the findings mean for you and whether follow-up testing or treatment is needed.
Abnormally high levels of C14-OH acylcarnitine in amniotic fluid may indicate that the baby has a disorder affecting fatty acid oxidation, such as multiple acyl-CoA dehydrogenase deficiency (MADD) or long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD). These are rare but serious conditions that affect how the body converts fat into energy. Your healthcare provider will interpret these results in combination with other test results and discuss any necessary follow-up steps with you.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Elevated C14-OH acylcarnitine in amniotic fluid is primarily associated with fetal fatty acid oxidation disorders. These inherited metabolic conditions can lead to serious health problems if not diagnosed and treated early. Common conditions detected include multiple acyl-CoA dehydrogenase deficiency (MADD) and long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD), which are types of mitochondrial fatty acid oxidation disorders. Early diagnosis allows for immediate dietary management and treatment after birth, which can significantly improve outcomes. This test is often part of a broader acylcarnitine profile panel performed on amniotic fluid for comprehensive metabolic screening.
Frequently asked questions
Is this test part of routine pregnancy care?
How is the amniotic fluid sample collected?
What happens if the results are abnormal?
Can these metabolic disorders be treated?
Sources
- 1
- 2
- 3
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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