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ACADL Gene LCAD deficiency NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

ACADL Gene LCAD deficiency NGS Genetic Test

Short Name: ACADL Gene Test

Also known as: LCAD deficiency genetic test, ACADL gene sequencing, Fatty acid oxidation disorder test

ACADL Gene LCAD deficiency NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing on Blood samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the ACADL gene that cause LCAD deficiency, enabling early diagnosis, management, and genetic counseling for affected individuals and families.

Test Code
2122
Price
₹20,000
Sample Type
Blood
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing
Step 1

Sample Collection

No special preparation required. Inform the healthcare provider about any medications or medical conditions.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm using standard venipuncture techniques.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless otherwise advised.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor to discuss family history and test implications.
2
During the Test:Blood draw procedure takes approximately 10-15 minutes.
3
After the Test:Results will be available in 3-4 weeks. Genetic counseling is provided post-test for interpretation.

About This Test

Who Should Get This Test

To detect mutations in the ACADL gene that cause LCAD deficiency, enabling early diagnosis, management, and genetic counseling for affected individuals and families.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection tubes
  • Label samples accurately
  • Transport at ambient temperature

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Early genetic diagnosis of LCAD deficiency is crucial for preventing metabolic crises and guiding personalized treatment plans to improve patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 24 hours at room temperature
Store at 2-8°C if delayed processing
Sample Rejection Criteria:
  • Hemolyzed or lipemic samples
  • Insufficient volume
  • Improper labeling or contamination

Understanding Your Results

Results from the ACADL Gene NGS Test are interpreted by genetic specialists to identify mutations linked to LCAD deficiency.
Positive result: Indicates presence of a pathogenic variant in the ACADL gene, confirming LCAD deficiency.
Negative result: Suggests no known pathogenic variants detected, but does not rule out all mutations.
Variant of uncertain significance: Requires further testing or family studies for clarification.
⚠️ When to Consult a Doctor:

If you experience symptoms like recurrent hypoglycemia, muscle weakness, or have a family history of metabolic disorders, consult a geneticist or metabolic specialist immediately.

Limitations

  • May not detect all genetic variants
  • Cannot predict disease severity
  • Results require clinical correlation

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection
  • Psychological impact of genetic results

Interfering Factors

  • Hemolyzed blood samples
  • Recent blood transfusions
  • Contaminated samples

Frequently Asked Questions

What is the ACADL Gene LCAD Deficiency NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to detect mutations in the ACADL gene, which can lead to LCAD deficiency, a fatty acid metabolism disorder.
What is LCAD deficiency?
LCAD deficiency is a rare genetic disorder where the body cannot properly break down fatty acids for energy, causing symptoms like muscle weakness and hypoglycemia.
Who should consider this test?
Individuals with symptoms of LCAD deficiency, family history of metabolic disorders, or those with unexplained hypoglycemia or muscle problems.
What are the common symptoms of LCAD deficiency?
Symptoms include muscle weakness, fatigue, low blood sugar, abdominal pain, liver issues, and in severe cases, seizures or heart enlargement.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to identify genetic mutations in the ACADL gene.
What is the cost of the test?
The test costs INR 20,000, which includes genetic counseling and support services.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test across many cities in India.
What does a positive result mean?
A positive result indicates a mutation in the ACADL gene, confirming a diagnosis of LCAD deficiency and guiding treatment decisions.
Can this test diagnose other conditions?
No, it specifically targets mutations related to LCAD deficiency, but related tests can assess other fatty acid oxidation disorders.
Is genetic counseling included in the test?
Yes, genetic counseling is provided before and after the test to help interpret results and discuss implications.
How accurate is the test?
The NGS technology used is highly accurate, with the ability to detect rare mutations, but results should be correlated with clinical evaluation.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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