Skip to content

3ohpalmitoylcarnamnscnc

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

A prenatal blood test that measures C16-OH levels in amniotic fluid to screen for fetal fatty acid oxidation disorders.

Quick summary

{"This test measures 3-Hydroxypalmitoylcarnitine (C16-OH) levels in amniotic fluid during pregnancy","It helps screen for fatty acid oxidation disorders in the unborn baby, such as MCAD deficiency","Abnormally high levels may indicate the baby has a metabolic disorder that requires special care after birth","The test is part of newborn screening but performed during pregnancy for early diagnosis","If abnormal, doctors will discuss treatment options and delivery planning"}

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

Key facts at a glance

LOINC
50126-2
Short code
3OH-Palmitoylcarn Amn-sCnc
Synonyms
3OH-Palmitoylcarn 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 3-Hydroxypalmitoylcarnitine (C16-OH) test measures the amount of a specific fatty acid substance in the amniotic fluid that surrounds the baby during pregnancy. C16-OH is a type of acylcarnitine that can build up in the blood when the body cannot properly break down fats for energy. This test helps doctors determine if the unborn baby may have a fatty acid oxidation disorder.

Why is this test done during pregnancy?

This test is performed during pregnancy to screen for inherited metabolic disorders, particularly Medium-Chain Acyl-CoA Dehydrogenase (MCAD) deficiency and other fatty acid oxidation disorders. These conditions prevent the body from converting fats into energy properly. Early detection allows healthcare providers to prepare for special care needs after birth, including dietary management and avoidance of fasting, which can prevent serious complications.

How is the test performed?

During amniocentesis, a thin needle is used to collect a small sample of amniotic fluid from the womb. The sample is then sent to a laboratory where the C16-OH level is measured. The procedure is typically performed between 15-20 weeks of pregnancy, though timing may vary based on individual circumstances.

What do the results mean?

Normal C16-OH levels in amniotic fluid indicate no evidence of a fatty acid oxidation disorder. Elevated levels suggest the unborn baby may have a metabolic condition. However, follow-up testing after birth is usually needed to confirm the diagnosis. If results are abnormal, a genetic counselor or metabolic specialist will discuss the implications and create a management plan for the baby's care.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Frequently asked questions

Is this test safe for my baby?
Amniocentesis, the procedure used to collect the sample, carries a small risk of miscarriage (about 1 in 300-500). Your healthcare provider will discuss the risks and benefits based on your specific situation.
What happens if the test shows high C16-OH levels?
If results are abnormal, your doctor will likely recommend additional testing after birth to confirm the diagnosis. The healthcare team will also discuss special care plans, including dietary modifications and monitoring protocols to keep your baby healthy.
Can this test detect all metabolic disorders?
No, this test specifically screens for fatty acid oxidation disorders like MCAD deficiency. Other conditions require different tests. Newborn screening after birth will check for a broader range of disorders.
Do I need to fast before this test?
No fasting is required for this test. However, inform your doctor about any medications or supplements you are taking, as these may affect the results.
What is the difference between this prenatal test and newborn screening?
This prenatal test uses amniotic fluid collected during pregnancy to screen for disorders before birth. Newborn screening is performed after birth using a blood sample from the baby's heel. The prenatal test allows for earlier preparation, while newborn screening provides definitive diagnosis.
  1. 1
  2. 2
  3. 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.

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