LYRM4 Gene Combined oxidative phosphorylation deficiency type 19 NGS Genetic Test
Short Name: LYRM4 COXPD19 NGS Test
Also known as: COXPD19 NGS Test, LYRM4 Gene Mutation Test
LYRM4 Gene Combined oxidative phosphorylation deficiency type 19 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.
🩺 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 diagnose COXPD19 by detecting mutations in the LYRM4 gene using NGS technology, enabling accurate diagnosis and informed clinical management.
- Test Code
- 1934
- 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)
Sample Collection
No specific preparation required. Clinical history and genetic counseling are recommended.
Method: Venipuncture or FTA card application
Laboratory Analysis
Blood sample collected via venipuncture or FTA card application by a trained professional.
Report Delivery
Sample labeled and transported to the lab under stable conditions.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to diagnose COXPD19 by detecting mutations in the LYRM4 gene using NGS technology, enabling accurate diagnosis and informed clinical management.
How to Prepare
- Use EDTA tube for blood samples
- Avoid hemolysis during collection
- Store FTA card at room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for COXPD19 can facilitate timely intervention, management, and genetic counseling for affected families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Contaminated or hemolyzed samples
- Incorrect labeling
Understanding Your Results
If symptoms such as developmental delay, seizures, or lactic acidosis are present, consult a geneticist or healthcare provider for evaluation.
Limitations
- ⚠May not detect all types of mutations
- ⚠Results require genetic counseling for interpretation
Risks & Considerations
- ●Psychological impact of results
- ●Potential for incidental findings
- ●Standard blood draw risks
Interfering Factors
- ●Poor sample quality
- ●DNA contamination
- ●Hemolyzed blood samples
Frequently Asked Questions
What is COXPD19?
How is the test performed?
What is the cost of the test?
Who should get this test?
How accurate is the NGS test?
What sample is required?
Is fasting required?
How long does it take to get results?
Is home collection available?
What do the results mean?
Can this test be used for prenatal diagnosis?
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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.
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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