PRKCSH Gene Polycystic liver disease NGS Genetic Test
Short Name: PRKCSH PLD NGS Test
Also known as: PRKCSH Gene Test, Polycystic Liver Disease Genetic Test, PLD NGS Test
PRKCSH Gene Polycystic liver disease 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 SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
To diagnose mutations in the PRKCSH gene associated with polycystic liver disease, enabling early detection, risk assessment, and informed management decisions.
- Test Code
- 5485
- 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 special preparation is required. Provide clinical history and family pedigree as advised.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in the arm using standard venipuncture technique.
Report Delivery
Apply pressure to the puncture site to stop bleeding. Resume normal activities unless otherwise directed.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose mutations in the PRKCSH gene associated with polycystic liver disease, enabling early detection, risk assessment, and informed management decisions.
How to Prepare
- Ensure proper patient identification
- Use sterile collection equipment
- Label samples correctly
- Transport samples at ambient temperature as per guidelines
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"This test is crucial for early diagnosis and management of polycystic liver disease, especially in individuals with a family history or symptoms. Genetic counseling is recommended post-test."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Incorrect sample container
- Contaminated or hemolyzed samples
Understanding Your Results
Mutation Detected
Pathogenic variant in PRKCSH gene identified, associated with increased risk of polycystic liver disease. Genetic counseling and clinical follow-up recommended.
No Mutation Detected
No pathogenic variants found in PRKCSH gene. Risk of PLD due to this gene is low, but other genetic or environmental factors may be involved.
Variant of Uncertain Significance
A genetic variant was found but its clinical significance is unknown. Further testing and consultation may be needed.
If you experience symptoms of polycystic liver disease, have a family history of the condition, or receive a positive test result, consult a healthcare provider or genetic counselor for personalized advice.
Limitations
- ⚠May not detect all types of mutations or variants of uncertain significance
- ⚠Results require interpretation by a qualified geneticist or healthcare provider
- ⚠Does not rule out other genetic causes of liver disease
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection at puncture site
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Hemolyzed blood samples
Compare With Similar Tests
| Test | PRKCSH Gene Polycystic liver disease NGS Genetic Test | ||||
|---|---|---|---|---|---|
| Comparison | PRKCSH Gene Polycystic liver disease NGS Genetic Test |
Frequently Asked Questions
What is the PRKCSH Gene Polycystic Liver Disease NGS Genetic Test?
How much does the test cost?
What sample is required for the test?
How long does it take to get results?
Is home collection available?
What are the symptoms of polycystic liver disease?
How is polycystic liver disease diagnosed?
What is the role of the PRKCSH gene in PLD?
Is the test covered by insurance?
What should I do if I have a family history of PLD?
How accurate is the NGS genetic test?
What are the risks of the test?
Related Tests
NR1H4 Gene Cholestasis, infantile, NR1H4 related NGS Genetic Test
₹20,000UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic Test
₹20,000UGT1A1 Gene Crigler-Najjar syndrome, type 2 NGS Genetic Test
₹20,000ABCC2 Gene Dubin-Johnson syndrome NGS Genetic Test
₹20,000NBAS Gene Infantile liver failure syndrome type 2 NGS Genetic Test
₹20,000Criggler Najjar Syndrome
₹27,000Reference 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.
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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
