ROR2 Gene Brachydactyly type B1 NGS Genetic Test
Short Name: ROR2 Brachydactyly B1 NGS Test
Also known as: Brachydactyly Type B1, ROR2-Related Brachydactyly
ROR2 Gene Brachydactyly type B1 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To identify pathogenic mutations in the ROR2 gene for diagnosis of brachydactyly type B1 and to guide clinical management.
- Test Code
- 5685
- 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 recommended. Provide clinical history and family pedigree.
Method: Venipuncture or FTA card spotting
Laboratory Analysis
Blood sample collected via venipuncture or FTA card.
Report Delivery
Sample sent to lab for NGS analysis.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic mutations in the ROR2 gene for diagnosis of brachydactyly type B1 and to guide clinical management.
How to Prepare
- Ensure proper labeling
- Use sterile equipment
- Follow aseptic techniques
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This NGS test is essential for confirming ROR2 gene mutations, aiding in precise diagnosis and personalized management of brachydactyly type B1."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient volume
- Improperly labeled samples
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of brachydactyly type B1
No pathogenic variant detected
Reduces likelihood, but clinical correlation needed
If symptoms of brachydactyly are present or if there is a family history of the condition.
Limitations
- ⚠May not detect all types of mutations
- ⚠Requires genetic counseling for interpretation
- ⚠Results may have implications for family members
Risks & Considerations
- ●Minor bruising at blood draw site
- ●Rare infection risk
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample handling
Compare With Similar Tests
| Test | ROR2 Gene Brachydactyly type B1 NGS Genetic Test | Sanger Sequencing | Clinical Examination |
|---|---|---|---|
| Comparison | ROR2 Gene Brachydactyly type B1 NGS Genetic Test |
Frequently Asked Questions
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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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