TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic Test
Short Name: TRIM32 BBS Type 11 NGS Test
Also known as: Bardet-Biedl Syndrome Type 11, BBS Type 11, TRIM32-related BBS
TRIM32 Gene Bardet-Biedl syndrome type 11 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 from sample receipt. 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
To diagnose Bardet-Biedl Syndrome Type 11 by detecting mutations in the TRIM32 gene using Next-Generation Sequencing (NGS) technology, enabling accurate diagnosis and management.
- Test Code
- 5374
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks from sample receipt
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
Provide detailed clinical history and family pedigree during genetic counseling session.
Method: Venipuncture or Saliva Collection
Laboratory Analysis
Blood draw via venipuncture or saliva sample collection using sterile equipment.
Report Delivery
Sample is labeled and transported to the laboratory under ambient conditions for analysis.
Timeline: 3 to 4 weeks from sample receipt
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Bardet-Biedl Syndrome Type 11 by detecting mutations in the TRIM32 gene using Next-Generation Sequencing (NGS) technology, enabling accurate diagnosis and management.
How to Prepare
- Use sterile collection tubes or FTA cards
- Label samples with patient details and date
- Avoid contamination during collection
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"As an OB-GYN, I recommend genetic counseling for families with a history of Bardet-Biedl Syndrome to assess reproductive risks and guide management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improperly labeled or contaminated samples
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of BBS Type 11; recommend genetic counseling and symptom management.
No pathogenic variant detected
BBS Type 11 unlikely based on TRIM32 gene; clinical correlation and further testing may be needed.
If symptoms of Bardet-Biedl Syndrome are present, such as vision problems, obesity, or developmental delays, or if there is a family history of genetic disorders.
Limitations
- ⚠May not detect all genetic variants or mosaicism
- ⚠Requires genetic counseling for accurate interpretation
- ⚠Results may not predict disease severity or onset
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Psychological impact of genetic results on patients and families
Interfering Factors
- ●Poor sample quality or contamination
- ●Hemolyzed blood samples
- ●Improper storage or handling of samples
Compare With Similar Tests
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| Comparison | TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic Test |
Frequently Asked Questions
What is the cost of the TRIM32 Gene BBS Type 11 NGS Test?
How is the test performed?
What samples are required for the test?
Is fasting required before the test?
How long does it take to get results?
Is home sample collection available?
What are the symptoms of BBS Type 11?
How accurate is the NGS test?
Can this test be used for prenatal diagnosis?
What if the test is positive?
Is genetic counseling included?
Are there any risks associated with the test?
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₹20,000Reference 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.
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