CCDC103 Gene Primary ciliary dyskinesia type 17 NGS Genetic Test
Short Name: CCDC103 PCD Type 17 NGS Test
Also known as: PCD Type 17 Genetic Test, CCDC103 Gene Analysis
CCDC103 Gene Primary ciliary dyskinesia type 17 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 diagnose Primary Ciliary Dyskinesia Type 17 by identifying mutations in the CCDC103 gene using Next-Generation Sequencing (NGS) technology.
- Test Code
- 4772
- 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
No specific preparation required. Provide detailed clinical history and family pedigree during genetic counseling.
Method: Venipuncture or FTA Card
Laboratory Analysis
A blood sample will be collected via venipuncture or using an FTA card for DNA extraction.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Primary Ciliary Dyskinesia Type 17 by identifying mutations in the CCDC103 gene using Next-Generation Sequencing (NGS) technology.
How to Prepare
- Ensure proper patient identification
- Use sterile collection equipment
- Label samples accurately with patient details
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This genetic test is crucial for diagnosing Primary Ciliary Dyskinesia Type 17, helping in early management and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improper labeling or documentation
Understanding Your Results
Positive
Pathogenic variant detected, consistent with PCD Type 17. Consult a genetic counselor for management and family implications.
Negative
No pathogenic variants detected. Clinical correlation with symptoms and other diagnostic tests is recommended.
Variant of Uncertain Significance (VUS)
Further testing, family studies, or functional assays may be needed for clarification.
If symptoms persist despite treatment, or if there is a family history of PCD, consult a geneticist or pulmonologist for further evaluation.
Limitations
- ⚠May not detect all genetic variants or non-coding region mutations
- ⚠Requires genetic counseling for accurate interpretation
- ⚠Not a standalone diagnostic tool; clinical correlation with other tests is recommended
Risks & Considerations
- ●Minimal risks from blood draw: bruising, soreness, or rare infection
- ●Potential psychological impact of genetic results; counseling is provided
Compare With Similar Tests
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|---|---|---|---|---|
| Comparison | CCDC103 Gene Primary ciliary dyskinesia type 17 NGS Genetic Test |
Frequently Asked Questions
What is the CCDC103 Gene Primary Ciliary Dyskinesia Type 17 NGS Genetic Test?
What are the common symptoms of Primary Ciliary Dyskinesia?
How is PCD diagnosed besides genetic testing?
What is the cost of this test at DNA Labs India?
Is home sample collection available for this test?
How long does it take to receive the test results?
What does a positive test result mean?
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Is genetic counseling provided with this test?
Can this test be used for prenatal diagnosis?
What are the limitations of this genetic test?
How accurate is the CCDC103 Gene NGS Genetic Test?
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