PDCD10 Gene Cerebral cavernous malformations type 3 NGS Genetic Test
Short Name: PDCD10 Gene CCM Type 3 NGS Test
Also known as: CCM3 Genetic Test, PDCD10 Mutation Analysis
PDCD10 Gene Cerebral cavernous malformations type 3 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 identify mutations in the PDCD10 gene associated with cerebral cavernous malformations type 3, aiding in diagnosis, genetic counseling, and management of the condition.
- Test Code
- 5319
- 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
Genetic counseling is recommended prior to testing. Provide detailed clinical and family history.
Method: Venipuncture
Laboratory Analysis
A blood sample will be collected via venipuncture by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Store sample as instructed.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify mutations in the PDCD10 gene associated with cerebral cavernous malformations type 3, aiding in diagnosis, genetic counseling, and management of the condition.
How to Prepare
- Ensure patient identification is correct
- Use sterile equipment
- Label sample properly with patient details
- Transport sample at ambient room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for PDCD10 gene mutations is essential for early diagnosis and management of cerebral cavernous malformations type 3, especially in families with a history of vascular diseases."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect sample type or container
- Missing patient information
Understanding Your Results
Consult a doctor if you experience symptoms like seizures, headaches, or neurological deficits, or if you have a family history of cerebral cavernous malformations.
Limitations
- ⚠May not detect all types of mutations, such as large deletions or duplications
- ⚠Results may include variants of uncertain significance (VUS)
- ⚠Does not rule out other genetic or non-genetic causes of symptoms
Risks & Considerations
- ●Minor bruising or pain at the blood draw site
- ●Rare risk of infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Contaminated or degraded DNA sample
- ●Improper sample storage or handling
- ●Recent blood transfusion
Compare With Similar Tests
| Test | PDCD10 Gene Cerebral cavernous malformations type 3 NGS Genetic Test | MRI Brain | CT Scan | EEG |
|---|---|---|---|---|
| Comparison | PDCD10 Gene Cerebral cavernous malformations type 3 NGS Genetic Test |
Frequently Asked Questions
What is the PDCD10 Gene Cerebral Cavernous Malformations Type 3 NGS Genetic Test?
What are the symptoms of CCM type 3?
How is CCM type 3 diagnosed?
What is the cost of this genetic test in India?
Is fasting required for this test?
What sample types are accepted?
How long does it take to get results?
Is home sample collection available?
What does a positive result mean?
Can this test be used for family planning?
Are there any risks associated with the test?
What should I do if I have symptoms?
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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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