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DNA Labs India

PLN Gene Cardiomyopathy, dilated type 1P NGS Genetic Test

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PLN Gene Cardiomyopathy, dilated type 1P NGS Genetic Test

Short Name: PLN Cardiomyopathy Test

Also known as: PLN Gene Cardiomyopathy, Dilated Cardiomyopathy 1P, PLN-Related Cardiomyopathy

PLN Gene Cardiomyopathy, dilated type 1P NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) 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

🩺 Medically Reviewed By

Overview

The purpose of the PLN Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the PLN gene that cause dilated cardiomyopathy type 1P. This helps in accurate diagnosis, risk assessment for family members, and guiding treatment decisions.

Test Code
5225
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
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree.

Method: Venipuncture for blood sample

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture. For FTA card, a drop of blood is applied.

Step 3

Report Delivery

Apply pressure to the puncture site. Resume normal activities.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a healthcare provider for genetic counseling. Provide family medical history.
2
During the Test:Sample collection is quick and minimally invasive. The test involves NGS technology to analyze the PLN gene.
3
After the Test:Results are available in 3-4 weeks. Follow-up with a genetic counselor for interpretation.

About This Test

Who Should Get This Test

The purpose of the PLN Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the PLN gene that cause dilated cardiomyopathy type 1P. This helps in accurate diagnosis, risk assessment for family members, and guiding treatment decisions.

How to Prepare

  • Bring identification and doctor's prescription
  • Inform about any medications
  • Ensure sample is properly labeled

Doctor's Notes

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

"Genetic testing for PLN gene mutations is crucial for early detection and management of dilated cardiomyopathy, especially in families with a history of heart disease."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture for blood sample

Sample Stability

Blood samples: stable for 48 hours at room temperature
Extracted DNA: stable for longer periods at -20°C
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Incorrect labeling
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of mutations in the PLN gene. A positive result confirms genetic predisposition to dilated cardiomyopathy type 1P.
📊

Positive for pathogenic variant

Confirms diagnosis of PLN gene cardiomyopathy. Genetic counseling recommended.

📊

Negative for pathogenic variant

No mutation detected. Clinical correlation advised.

📊

Variant of uncertain significance

Further testing and family studies may be needed.

⚠️ When to Consult a Doctor:

If you have a family history of heart disease, experience symptoms like shortness of breath or fatigue, or if test results are positive, consult a cardiologist or genetic counselor.

Limitations

  • May not detect all genetic variants
  • Results require interpretation by a genetic counselor
  • Does not rule out other causes of cardiomyopathy

Risks & Considerations

  • Minimal physical risk from blood draw
  • Potential psychological impact of genetic results
  • Risk of incidental findings

Interfering Factors

  • Poor sample quality
  • Contamination during sample handling
  • Insufficient DNA quantity

Compare With Similar Tests

TestPLN Gene Cardiomyopathy, dilated type 1P NGS Genetic TestEchocardiogramCardiac MRIECGOther Genetic Panels
ComparisonPLN Gene Cardiomyopathy, dilated type 1P NGS Genetic TestAssesses heart structure and function but does not identify genetic cause.Provides detailed heart imaging but not genetic analysis.Monitors heart rhythm but not specific for genetic mutations.May include multiple genes; PLN test is specific for this gene.

Frequently Asked Questions

What is PLN Gene Cardiomyopathy?
PLN Gene Cardiomyopathy is a rare genetic form of dilated cardiomyopathy caused by mutations in the PLN gene, affecting heart muscle function.
What are the symptoms of PLN Gene Cardiomyopathy?
Symptoms include shortness of breath, fatigue, chest pain, swelling in legs, and irregular heartbeat. Some individuals may be asymptomatic.
How is PLN Gene Cardiomyopathy diagnosed?
Diagnosis is through genetic testing, specifically NGS, to identify mutations in the PLN gene, often supplemented with cardiac imaging.
What is the cost of the PLN Gene Cardiomyopathy NGS Genetic Test?
The test costs INR 20000 at DNA Labs India, with free home sample collection available across India.
What sample is required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card is required.
How long does it take to get the results?
Results are typically available in 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across numerous cities in India.
What does a positive test result mean?
A positive result indicates a mutation in the PLN gene, confirming genetic predisposition to dilated cardiomyopathy type 1P. Genetic counseling is recommended.
Can this test be done for children?
Yes, the test can be performed on individuals of all ages, but genetic counseling is advised for minors.
Is genetic counseling provided?
Yes, a genetic counseling session is included to draw a pedigree chart and discuss results and implications.
What are the risks of the test?
Risks are minimal, including slight discomfort from blood draw and potential psychological impact of genetic results.
How accurate is the NGS Genetic Test?
NGS is highly accurate for detecting mutations, but results should be interpreted by a genetic counselor in clinical context.
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 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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