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PRKCH Gene Cerebral Infarction, Susceptibility to NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

PRKCH Gene Cerebral Infarction, Susceptibility to NGS Genetic Test

Short Name: PRKCH Genetic Test

Also known as: Ischemic Stroke Genetic Test, PRKCH Gene Susceptibility Test, Stroke Risk Genetic Test

PRKCH Gene Cerebral Infarction, Susceptibility to 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 Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to analyze DNA for variations in the PRKCH gene that may indicate an increased susceptibility to cerebral infarction (ischemic stroke). It aids in risk assessment, genetic counseling, and personalized prevention strategies.

Test Code
4553
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

No special preparation is required. Avoid eating, drinking, or smoking for at least 30 minutes before cheek swab collection to ensure sample integrity.

Method: Cheek Swab or Blood Draw

Step 2

Laboratory Analysis

Sample is collected via a non-invasive cheek swab or a standard blood draw by a trained phlebotomist.

Step 3

Report Delivery

The sample is securely packaged and sent to the laboratory for NGS analysis. Results are typically available in 3 to 4 weeks.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:No fasting required. Provide clinical history and undergo genetic counseling if recommended.
2
During the Test:Sample collection takes a few minutes via cheek swab or blood draw.
3
After the Test:Resume normal activities. Await results in 3-4 weeks.

About This Test

Who Should Get This Test

The purpose of this test is to analyze DNA for variations in the PRKCH gene that may indicate an increased susceptibility to cerebral infarction (ischemic stroke). It aids in risk assessment, genetic counseling, and personalized prevention strategies.

How to Prepare

  • For cheek swab: Rinse mouth with water 30 minutes prior, avoid food/drink
  • For blood sample: Follow standard phlebotomy procedures
  • Ensure proper labeling of sample with patient details
  • Store sample at ambient temperature if not processed immediately

Doctor's Notes

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

"Genetic testing for PRKCH gene variations can help identify individuals at increased risk for cerebral infarction, enabling personalized preventive measures and early intervention strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodCheek Swab or Blood Draw

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for up to 1 week at 2-8°C or longer if frozen
Sample Rejection Criteria:
  • Insufficient sample volume
  • Contaminated or hemolyzed sample
  • Improperly labeled or unlabeled sample
  • Sample received beyond stability period

Understanding Your Results

Results indicate the presence or absence of genetic variations in the PRKCH gene associated with cerebral infarction susceptibility. Consult a genetic counselor or healthcare provider for personalized interpretation.
📊

Positive for susceptibility variants

Increased genetic risk for cerebral infarction. Recommend lifestyle modifications, regular monitoring, and consultation with a neurologist or genetic counselor.

📊

Negative for susceptibility variants

No increased genetic risk detected based on PRKCH gene analysis. Continue standard preventive measures for stroke.

📊

Variant of uncertain significance (VUS)

Genetic variation found but clinical significance is unknown. Further testing or family studies may be recommended.

⚠️ When to Consult a Doctor:

If you have a family history of stroke, experience symptoms of cerebral infarction (e.g., sudden weakness, numbness, speech difficulties), or receive a positive test result, consult a neurologist or genetic counselor promptly.

Limitations

  • This test assesses genetic susceptibility only and does not diagnose cerebral infarction
  • Risk prediction is probabilistic and not definitive
  • Other genetic, environmental, and lifestyle factors also contribute to stroke risk
  • Results should be interpreted in conjunction with clinical evaluation and family history

Risks & Considerations

  • Minimal physical risk from sample collection (e.g., slight discomfort from blood draw)
  • Potential psychological impact of learning genetic risk information
  • Risk of misinterpretation without professional guidance

Interfering Factors

  • Sample contamination
  • Degraded DNA quality
  • Technical errors in sequencing or analysis
  • Improper sample collection or storage

Frequently Asked Questions

What is the PRKCH gene?
The PRKCH gene is involved in regulating blood vessel function and inflammation. Variations in this gene have been linked to an increased risk of cerebral infarction (ischemic stroke).
Who should consider this genetic test?
Individuals with a family history of stroke, personal risk factors like hypertension or diabetes, or those seeking preventive health assessment may benefit from this test.
How is the test performed?
The test uses NGS technology to analyze DNA from a cheek swab or blood sample. It is non-invasive and performed in a laboratory setting.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, which includes sample collection, analysis, and a detailed report.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate whether you have genetic variations in the PRKCH gene that may increase your risk of cerebral infarction. A positive result suggests higher susceptibility, while negative means no increased risk detected.
Is the test painful?
No, the test involves a simple cheek swab or blood draw, which may cause minimal discomfort but is generally painless.
Can this test diagnose stroke?
No, this test assesses genetic susceptibility only. It does not diagnose cerebral infarction or stroke; diagnosis requires clinical evaluation and imaging tests.
What should I do after receiving results?
Consult a healthcare provider or genetic counselor to interpret results and discuss personalized prevention strategies, such as lifestyle changes or monitoring.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing to understand implications, especially if there is a family history of stroke.
Are there any risks associated with the test?
Risks are minimal, including slight discomfort from sample collection and potential psychological impact of results. Professional guidance is recommended for interpretation.
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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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.

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