Fatty Acid Levels: Determining concentrations of short-, medium-, and long-chain fatty acids in the blood. Diagnosis of Metabolic Disorders: Such as fatty acid enzyme deficiencies, which may lead to various health problems, including growth impairment and organ dysfunction. Genetic Mutation Identification: In some cases, the test may reveal indicators that help identify hereditary conditions affecting fatty acid metabolism. Health Risk Assessment: The test helps evaluate risks related to overall health, such as cardiovascular diseases.

Individuals with Unexplained Symptoms: Such as muscle weakness, growth problems, or organ function disorders. Newborns: Especially when there is suspicion of hereditary metabolic disorders, such as fatty acid enzyme deficiencies. Individuals with a Family History: Those with family members affected by metabolic disorders or similar hereditary conditions. People with Chronic Health Issues: Such as heart disease or diabetes, as fatty acid levels may be related to overall health status. Individuals Experiencing Recurrent Symptoms: Such as episodes of muscle pain or unexplained fatigue.

Muscle Weakness: Unexplained fatigue or weakness in the muscles. Growth Problems: Delayed physical or mental development in children. Recurrent Pain Episodes: Such as muscle pain or cramps. Chronic Fatigue: Persistent tiredness and exhaustion despite adequate rest. Organ Function Disorders: Such as liver or heart problems, which may indicate metabolic dysfunction. Family History of Metabolic Disorders: Presence of family members with similar conditions or hereditary diseases.

What is the Fatty Acid Disorders Test? It is a test used to determine fatty acid levels in the blood to diagnose related metabolic disorders. Why is this test performed? To diagnose metabolic disorders such as fatty acid enzyme deficiencies, or to assess health risks associated with fatty acids. How is the test performed? A blood sample is drawn and analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Does the test require any special preparations? Usually, no preparations are needed, but it is recommended to consult the doctor regarding any medications or supplements taken before the test. How long does it take to get results? Results typically appear within one to two weeks, depending on the laboratory. What are the risks associated with the test? Risks are minimal, including discomfort during the blood draw or minor bruising. What do the test results mean? Positive results indicate an imbalance in fatty acid levels, while negative results may indicate no apparent disorders.

Short-, Medium-, and Long-Chain Fatty Acid Levels: These are usually present in certain proportions, but exact values depend on the reference standards of each laboratory. Normal Results: Typically defined by the laboratory based on factors such as age, sex, and overall health status.

Fatty Acid Disorders Test Price | Lahalak Platform

Advanced analysis to measure blood fatty acid levels, aiding in early detection of metabolic disorders and ensuring efficient metabolism for better overall health and energy.

Prices starts from: 422.4 SAR

Scientific name: Fatty Acid Disorders Profile (LC-MS/MS)

The Fatty Acid Disorders (LC-MS/MS Tandem) test is an advanced laboratory test used to measure fatty acid levels in the blood, including short, medium, and long-chain fatty acids. This test is essential for diagnosing a range of metabolic disorders, such as deficiencies in fatty acid enzymes, which can lead to health problems like growth issues, mu...

Service type Laboratory Test (Blood)

Duration 10-15 minutes

Fasting 8-12 hours fasting

Prices Starting from 422.4 SAR

Included Services

Fatty Acid Disorders - LC-MS/MS Tandem Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Fatty Acid Levels: Determining concentrations of short-, medium-, and long-chain fatty acids in the blood.
Diagnosis of Metabolic Disorders: Such as fatty acid enzyme deficiencies, which may lead to various health problems, including growth impairment and organ dysfunction.
Genetic Mutation Identification: In some cases, the test may reveal indicators that help identify hereditary conditions affecting fatty acid metabolism.
Health Risk Assessment: The test helps evaluate risks related to overall health, such as cardiovascular diseases.

Recommended groups

Individuals with Unexplained Symptoms: Such as muscle weakness, growth problems, or organ function disorders.
Newborns: Especially when there is suspicion of hereditary metabolic disorders, such as fatty acid enzyme deficiencies.
Individuals with a Family History: Those with family members affected by metabolic disorders or similar hereditary conditions.
People with Chronic Health Issues: Such as heart disease or diabetes, as fatty acid levels may be related to overall health status.
Individuals Experiencing Recurrent Symptoms: Such as episodes of muscle pain or unexplained fatigue.

Symptoms indicative

Muscle Weakness: Unexplained fatigue or weakness in the muscles.
Growth Problems: Delayed physical or mental development in children.
Recurrent Pain Episodes: Such as muscle pain or cramps.
Chronic Fatigue: Persistent tiredness and exhaustion despite adequate rest.
Organ Function Disorders: Such as liver or heart problems, which may indicate metabolic dysfunction.
Family History of Metabolic Disorders: Presence of family members with similar conditions or hereditary diseases.

FAQs

What is the Fatty Acid Disorders Test? It is a test used to determine fatty acid levels in the blood to diagnose related metabolic disorders.
Why is this test performed? To diagnose metabolic disorders such as fatty acid enzyme deficiencies, or to assess health risks associated with fatty acids.
How is the test performed? A blood sample is drawn and analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS).
Does the test require any special preparations? Usually, no preparations are needed, but it is recommended to consult the doctor regarding any medications or supplements taken before the test.
How long does it take to get results? Results typically appear within one to two weeks, depending on the laboratory.
What are the risks associated with the test? Risks are minimal, including discomfort during the blood draw or minor bruising.

Normal Levels

Short-, Medium-, and Long-Chain Fatty Acid Levels: These are usually present in certain proportions, but exact values depend on the reference standards of each laboratory.
Normal Results: Typically defined by the laboratory based on factors such as age, sex, and overall health status.