PIK3CA Gene Cowden syndrome type 5 NGS Genetic Test
Also known as: Cowden Syndrome Type 5 Genetic Test, PIK3CA Mutation Analysis, Hereditary Cancer Syndrome Test
PIK3CA Gene Cowden syndrome type 5 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To diagnose Cowden Syndrome Type 5 by detecting mutations in the PIK3CA gene using Next-Generation Sequencing technology, aiding in early identification and management of associated cancer risks.
- Test Code
- 2860
- 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
Sample Collection
Provide detailed clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with Cowden Syndrome Type 5.
Laboratory Analysis
Your sample is analyzed using NGS in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Cowden Syndrome Type 5 by detecting mutations in the PIK3CA gene using Next-Generation Sequencing technology, aiding in early identification and management of associated cancer risks.
How to Prepare
- Ensure proper patient identification and documentation.
- Blood sample will be collected by a trained phlebotomist using standard venipuncture.
- For FTA card collection, follow specific instructions for applying one drop of blood.
- Maintain sample integrity during transport to the laboratory.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for PIK3CA mutations is crucial for diagnosing Cowden Syndrome Type 5, enabling proactive cancer surveillance and management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive for pathogenic PIK3CA mutation
Diagnosis of Cowden Syndrome Type 5 is likely. Consult a genetic counselor and oncologist for personalized cancer surveillance and management plans.
Negative for pathogenic PIK3CA mutation
No mutation detected. Clinical correlation is recommended; symptoms may be due to other causes. Consider repeat testing if clinical suspicion remains high.
Variant of uncertain significance (VUS)
A genetic variant was found but its clinical significance is unknown. Further testing and family studies may be needed. Genetic counseling is advised.
Consult a doctor if you experience symptoms such as persistent skin lesions, thyroid abnormalities, breast lumps, gastrointestinal polyps, or neurological issues, or if you have a family history of Cowden Syndrome or related cancers.
Risks & Considerations
- ●Minor pain or bruising at the blood draw site
- ●Rare risk of infection or hematoma
- ●Psychological impact of genetic results; counseling recommended
Frequently Asked Questions
What is Cowden Syndrome Type 5?
What causes Cowden Syndrome Type 5?
What are the common symptoms of Cowden Syndrome Type 5?
How is Cowden Syndrome Type 5 diagnosed?
What is the cost of the PIK3CA Gene Cowden Syndrome Type 5 NGS Genetic Test?
Is home sample collection available for this test?
How long does it take to get the test results?
Is the genetic test accurate?
Can this test be performed on children?
What should I do if the test result is positive?
Is genetic counseling required before testing?
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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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