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LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic Test

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LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic Test

Short Name: LMNA Heart-hand Syndrome NGS Test

LMNA Gene Heart-hand syndrome, Slovenian type 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 TestAll Ages🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

The purpose of the LMNA Gene Heart-hand Syndrome NGS Genetic Test is to identify pathogenic mutations in the LMNA gene responsible for causing heart-hand syndrome, aiding in definitive diagnosis, risk assessment, and informed clinical decision-making.

Test Code
5258
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

Provide detailed clinical history and family pedigree. Attend a genetic counseling session as recommended.

Step 2

Laboratory Analysis

Standard blood draw procedure using venipuncture. For FTA card, a single drop of blood is collected.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Store samples as per instructions.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session recommended. Provide clinical and family history details.
2
During the Test:Blood sample collection via venipuncture or FTA card. The process is minimally invasive.
3
After the Test:Results are analyzed in the lab. Genetic counseling is advised to discuss findings.

About This Test

Who Should Get This Test

The purpose of the LMNA Gene Heart-hand Syndrome NGS Genetic Test is to identify pathogenic mutations in the LMNA gene responsible for causing heart-hand syndrome, aiding in definitive diagnosis, risk assessment, and informed clinical decision-making.

How to Prepare

  • Provide comprehensive clinical history of the patient
  • Complete a genetic counseling session to draw a family pedigree chart
  • Ensure proper sample labeling and handling

Doctor's Notes

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

"Early genetic testing for LMNA mutations is crucial for accurate diagnosis, personalized management, and informed family planning in LMNA-related disorders."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Rejection Criteria:
  • Hemolyzed or lipemic samples
  • Insufficient sample volume
  • Incorrect sample type or container
  • Samples without proper identification

Understanding Your Results

Results from the LMNA Gene NGS Test indicate the presence or absence of pathogenic variants in the LMNA gene, which are associated with heart-hand syndrome.
📊

Pathogenic variant detected

Confirms diagnosis of LMNA Gene Heart-hand Syndrome. Consult a genetic counselor for management, surveillance, and family planning.

📊

No pathogenic variant detected

LMNA mutations not found. Clinical correlation and consideration of other genetic or non-genetic causes are recommended.

📊

Variant of uncertain significance (VUS)

Further testing, family studies, and clinical follow-up may be needed to clarify the variant's role.

⚠️ When to Consult a Doctor:

Consult a healthcare provider if you experience symptoms such as heart palpitations, hand abnormalities, or have a family history of genetic disorders. Genetic counseling is advised before and after testing.

Limitations

  • ⚠May not detect all types of genetic variants, such as large deletions or duplications
  • ⚠Requires genetic counseling for accurate interpretation of results
  • ⚠Results may have implications for family members, necessitating further testing

Risks & Considerations

  • ●Minor bruising or discomfort at the blood draw site
  • ●Rare risk of infection or bleeding
  • ●Potential emotional impact from genetic results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA quality
  • ●Incorrect sample type or handling

Frequently Asked Questions

What is LMNA Gene Heart-hand Syndrome, Slovenian Type?
It is a rare genetic disorder caused by mutations in the LMNA gene, affecting the heart and hands, leading to conditions like arrhythmias, cardiomyopathy, and hand abnormalities.
What are the common symptoms of this syndrome?
Symptoms include heart problems (e.g., arrhythmias, dilated cardiomyopathy), hand abnormalities (e.g., syndactyly, brachydactyly), skeletal issues, eye problems, muscle weakness, and hearing loss.
How is LMNA Gene Heart-hand Syndrome diagnosed?
Diagnosis involves clinical evaluation, genetic testing (NGS), and imaging studies like ECG and echocardiography to assess heart function and detect abnormalities.
What is the cost of the NGS Genetic Test for this syndrome?
The cost at DNA Labs India is INR 20000, which includes home sample collection across India.
Is the test covered by insurance?
This test may not be covered by insurance. Individuals often need to pay out-of-pocket. Check with your insurance provider for details.
How long does it take to get the test results?
Results are typically delivered within 3 to 4 weeks after sample collection.
What sample is required for the test?
The test requires blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Can the test be done at home?
Yes, free home sample collection is available for online bookings across many cities in India.
What should I do if the test results are positive?
Consult a genetic counselor or healthcare provider for management, surveillance, and family planning options.
Are there any risks associated with the test?
Risks are minimal and include minor bruising at the blood draw site, rare infection, and potential emotional impact from results.
How accurate is the NGS Genetic Test?
NGS is highly accurate for detecting genetic variants, but interpretation requires expert genetic counseling. It may not detect all mutation types.
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.

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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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