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FLNA Gene Cardiac valvular dysplesia, X-linked NGS Genetic Test

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FLNA Gene Cardiac valvular dysplesia, X-linked NGS Genetic Test

Short Name: FLNA Cardiac Valvular Dysplasia NGS Test

Also known as: FLNA Gene Test for Cardiac Valvular Dysplasia

FLNA Gene Cardiac valvular dysplesia, X-linked 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 Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

To identify mutations in the FLNA gene that cause cardiac valvular dysplasia, enabling accurate diagnosis, genetic counseling, and informed management of the condition.

Test Code
2510
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

Genetic counseling and clinical history review recommended. No specific fasting required.

Method: Venipuncture or Finger-prick

Step 2

Laboratory Analysis

Standard blood draw or finger-prick procedure for sample collection.

Step 3

Report Delivery

Sample is processed and sent to the laboratory for NGS analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor and provide clinical history.
2
During the Test:Blood sample collection via venipuncture or finger-prick.
3
After the Test:Await results for 3 to 4 weeks; follow up with healthcare provider.

About This Test

Who Should Get This Test

To identify mutations in the FLNA gene that cause cardiac valvular dysplasia, enabling accurate diagnosis, genetic counseling, and informed management of the condition.

How to Prepare

  • Bring valid ID and doctor's prescription
  • Ensure sample is collected properly to avoid contamination

Doctor's Notes

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

"Early genetic testing for FLNA mutations can guide management of cardiac valvular dysplasia and inform family planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or Finger-prick
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the FLNA gene. Genetic counseling is advised for interpretation.
📊

Pathogenic variant detected

Confirms diagnosis of FLNA-related cardiac valvular dysplasia

📊

No pathogenic variant detected

FLNA gene mutation not identified; consider other causes

📊

Variant of uncertain significance

Further testing or family studies may be needed

⚠️ When to Consult a Doctor:

If symptoms persist, family history is positive, or for genetic counseling after test results.

Limitations

  • ⚠May not detect all genetic variants
  • ⚠Requires interpretation by a genetic specialist

Risks & Considerations

  • ●Minor bruising at collection site
  • ●Rare risk of infection

Interfering Factors

  • ●Contaminated sample
  • ●Degraded DNA

Frequently Asked Questions

What is FLNA Gene Cardiac Valvular Dysplasia?
It is a genetic disorder caused by mutations in the FLNA gene, leading to malformation of heart valves and associated symptoms.
How is the NGS Genetic Test performed?
The test uses Next-Generation Sequencing to analyze the FLNA gene from a blood or DNA sample.
What is the cost of the test in India?
The test costs INR 20000, with free home sample collection available.
Is home collection available for this test?
Yes, free home sample collection is offered across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks.
What are the symptoms of this condition?
Symptoms include shortness of breath, chest pain, fatigue, and dizziness or fainting.
Who should consider this genetic test?
Individuals with a family history of cardiac valvular dysplasia, symptoms, or suspected X-linked inheritance.
Is genetic counseling required before the test?
Genetic counseling is recommended to understand the implications and draw a family pedigree chart.
What does a positive result mean?
A positive result confirms a pathogenic variant in the FLNA gene, indicating the disorder.
Are there any risks associated with the test?
Risks are minimal, such as minor bruising from blood draw.
How accurate is the NGS genetic test?
NGS technology provides high accuracy for detecting gene mutations, but interpretation by a specialist is essential.
Can this test be used for prenatal diagnosis?
Yes, it can be used for prenatal testing in families with known mutations, after genetic counseling.
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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For Hospitals & Clinics

Reference Laboratory Services

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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