LMNA Gene Cardiomyopathy, dilated with hypergonadotropic hypogonadism NGS Genetic Test
Short Name: LMNA Cardiomyopathy NGS Test
Also known as: LMNA-related dilated cardiomyopathy with hypogonadism, Lamin A/C cardiomyopathy test, LMNA genetic analysis for heart and reproductive disorders
LMNA Gene Cardiomyopathy, dilated with hypergonadotropic hypogonadism 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 Results are typically available within 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of this test is to identify mutations in the LMNA gene that cause dilated cardiomyopathy with hypergonadotropic hypogonadism, enabling accurate diagnosis, risk assessment, and personalized management strategies.
- Test Code
- 2529
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- Results are typically available within 3 to 4 weeks after sample receipt.
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn via venipuncture or a drop on FTA card. The process is quick and minimally invasive.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.
Timeline: Results are typically available within 3 to 4 weeks after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify mutations in the LMNA gene that cause dilated cardiomyopathy with hypergonadotropic hypogonadism, enabling accurate diagnosis, risk assessment, and personalized management strategies.
How to Prepare
- Ensure proper identification and labeling of samples
- Use sterile equipment for blood collection
- Store samples at recommended temperatures before transport
- Follow FTA card instructions if using that method
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is essential for early diagnosis and management of LMNA-related disorders, aiding in personalized treatment plans and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood samples
- Insufficient sample volume
- Improperly labeled or contaminated samples
- Samples without accompanying clinical information
Understanding Your Results
Pathogenic mutation detected
Confirms diagnosis of LMNA-related cardiomyopathy with hypogonadism. Genetic counseling and cardiac monitoring recommended.
Likely pathogenic mutation detected
High probability of disorder. Further clinical evaluation and family testing advised.
Variant of uncertain significance (VUS)
Uncertain clinical significance. Repeat testing or functional studies may be needed.
No mutations detected
LMNA mutations not identified. Consider other genetic or non-genetic causes.
Consult a doctor if you experience symptoms like heart palpitations, shortness of breath, fatigue, or reproductive issues, especially with a family history of genetic disorders. After receiving test results, seek genetic counseling for interpretation and management.
Limitations
- ⚠May not detect all types of LMNA mutations, such as large deletions or duplications
- ⚠Results require interpretation by a qualified geneticist
- ⚠Variants of uncertain significance may be identified, necessitating further studies
- ⚠Does not assess other genes associated with cardiomyopathy or hypogonadism
Risks & Considerations
- ●Minimal physical risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results, including anxiety or stress
- ●Potential for uncertain results requiring further testing
Interfering Factors
- ●Sample degradation or contamination
- ●Insufficient DNA quantity or quality
- ●Hemolyzed or improperly stored blood samples
- ●Technical errors during NGS sequencing
Compare With Similar Tests
| Test | LMNA Gene Cardiomyopathy, dilated with hypergonadotropic hypogonadism NGS Genetic Test | ||||
|---|---|---|---|---|---|
| Comparison | LMNA Gene Cardiomyopathy, dilated with hypergonadotropic hypogonadism NGS Genetic Test | Imaging test for heart structure; genetic test identifies underlying cause. | Measures electrical activity; genetic test detects mutations. | Assesses reproductive hormones; genetic test identifies genetic basis. | Detailed heart imaging; complementary to genetic testing. |
Frequently Asked Questions
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₹20,000Reference 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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