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FLCN Gene Pneumothorax, primary spontaneous NGS Genetic Test

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FLCN Gene Pneumothorax, primary spontaneous NGS Genetic Test

Short Name: FLCN Gene Pneumothorax NGS Test

Also known as: FLCN gene mutation test, Pneumothorax genetic test, BHD syndrome genetic test

FLCN Gene Pneumothorax, primary spontaneous NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic TestAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the FLCN gene associated with primary spontaneous pneumothorax, enabling early diagnosis, risk assessment, and informed management decisions.

Test Code
4762
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

No specific preparation required. Ensure informed consent and genetic counseling session if needed.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample is drawn via venipuncture from a vein in the arm. For FTA card, a finger prick may be used.

Step 3

Report Delivery

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

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Understand the test purpose through genetic counseling. Provide clinical and family history.
2
During the Test:Blood sample collection is quick and minimally invasive. The sample is sent to the lab for NGS analysis.
3
After the Test:Wait for results as per turnaround time. Discuss findings with a healthcare provider for next steps.

About This Test

Who Should Get This Test

To detect mutations in the FLCN gene associated with primary spontaneous pneumothorax, enabling early diagnosis, risk assessment, and informed management decisions.

How to Prepare

  • Fast for 4-6 hours if specified, though not typically required
  • Avoid strenuous activity before sample collection
  • Bring identification and test requisition form
  • Inform staff of any medications or health conditions

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early detection of FLCN mutations through NGS testing can help identify individuals at risk for pneumothorax, enabling proactive management and genetic counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5-10 ml
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Improperly labeled or contaminated sample
  • Sample older than stability period

Understanding Your Results

Results indicate the presence or absence of mutations in the FLCN gene. A positive result suggests a genetic predisposition to pneumothorax, while a negative result may not completely rule out genetic factors.
📊

Normal

No pathogenic variant detected in the FLCN gene. Reduced genetic risk for pneumothorax, but clinical correlation is advised.

📊

Abnormal

Pathogenic variant detected. Increased risk for primary spontaneous pneumothorax. Genetic counseling and further management recommended.

📊

Variant of Uncertain Significance (VUS)

A genetic variant was found, but its clinical significance is unknown. Repeat testing or family studies may be needed.

⚠️ When to Consult a Doctor:

If you experience symptoms like chest pain or shortness of breath, have a family history of pneumothorax, or receive an abnormal test result, consult a pulmonologist or geneticist immediately.

Limitations

  • May not detect all possible mutations in the FLCN gene
  • Results require interpretation by a genetic counselor or specialist
  • Does not rule out other causes of pneumothorax
  • Genetic testing has inherent limitations in predicting disease onset

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection
  • Psychological impact of genetic results
  • Possible need for further testing

Interfering Factors

  • Sample contamination
  • Improper sample storage or handling
  • Hemolyzed blood sample
  • Recent blood transfusion

Compare With Similar Tests

TestFLCN Gene Pneumothorax, primary spontaneous NGS Genetic TestChest X-rayCT Scan of ChestPulmonary Function TestBHD Syndrome Genetic Test
ComparisonFLCN Gene Pneumothorax, primary spontaneous NGS Genetic Test

Frequently Asked Questions

What is the FLCN gene?
The FLCN gene produces folliculin, a protein that regulates cell growth. Mutations can lead to conditions like pneumothorax.
What is primary spontaneous pneumothorax?
It is a condition where the lung collapses without an apparent cause, often due to genetic factors like FLCN mutations.
Who should consider this genetic test?
Individuals with a family history of pneumothorax, recurrent lung collapses, or symptoms like chest pain and shortness of breath.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to detect mutations in the FLCN gene.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the FLCN gene, increasing the risk for pneumothorax. Genetic counseling is recommended.
Is the test painful?
The test involves a standard blood draw, which may cause minor discomfort but is generally not painful.
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, free home collection is offered across many cities in India for online bookings.
What is the cost of the test?
The test costs INR 20,000, with possible discounts for online bookings.
Can pneumothorax be prevented with this test?
While the test identifies genetic risk, prevention involves monitoring and lifestyle adjustments based on medical advice.
Are there any risks to the test?
Risks are minimal, mainly related to blood draw, such as bruising. Psychological impacts of results should be considered.
What should I do after receiving results?
Consult a healthcare provider or genetic counselor to understand the implications and plan for management or further testing.
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.

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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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