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TRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

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.

Next-Generation Sequencing (NGS) Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

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)
Step 1

Sample Collection

Provide detailed clinical history and family pedigree during genetic counseling session.

Method: Venipuncture or Saliva Collection

Step 2

Laboratory Analysis

Blood draw via venipuncture or saliva sample collection using sterile equipment.

Step 3

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

1
Before the Test:Genetic counseling session recommended to discuss test implications and family history.
2
During the Test:Sample collection and processing in the laboratory using NGS technology.
3
After the Test:Report generation, delivery, and follow-up consultation for interpretation.

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 — 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 TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required for analysis
ContainerSterile tube or FTA card
Collection MethodVenipuncture or Saliva Collection

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable for up to 7 days at 4°C
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the TRIM32 gene, aiding in the diagnosis of Bardet-Biedl Syndrome Type 11.
📊

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.

⚠️ When to Consult a Doctor:

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

TestTRIM32 Gene Bardet-Biedl syndrome type 11 NGS Genetic Test
ComparisonTRIM32 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?
The test costs INR 20,000, including home sample collection across India.
How is the test performed?
It uses Next-Generation Sequencing (NGS) to analyze the TRIM32 gene from a blood or saliva sample.
What samples are required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, free home collection is offered in many cities across India.
What are the symptoms of BBS Type 11?
Symptoms include vision loss, obesity, intellectual disability, delayed speech, hand/foot abnormalities, kidney issues, and diabetes.
How accurate is the NGS test?
NGS is highly accurate for detecting gene mutations, but genetic counseling is recommended for interpretation.
Can this test be used for prenatal diagnosis?
It is primarily for postnatal diagnosis; consult a genetic counselor for prenatal options.
What if the test is positive?
A positive result confirms BBS Type 11, and management focuses on symptom treatment and genetic counseling.
Is genetic counseling included?
Yes, a genetic counseling session is part of the test process to draw a family pedigree and discuss results.
Are there any risks associated with the test?
Risks are minimal, such as bruising from blood draw, but psychological impacts should be considered.
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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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.

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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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