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CFAP298 Gene Primary ciliary dyskinesia type 26 NGS Genetic Test

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CFAP298 Gene Primary ciliary dyskinesia type 26 NGS Genetic Test

Short Name: CFAP298 Gene PCD Type 26 NGS Test

Also known as: Primary Ciliary Dyskinesia Type 26, PCD Type 26

CFAP298 Gene Primary ciliary dyskinesia type 26 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.

NGS Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To diagnose Primary Ciliary Dyskinesia Type 26 by identifying mutations in the CFAP298 gene through next-generation sequencing.

Test Code
4781
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
NGS Technology
Step 1

Sample Collection

Genetic counseling and clinical history review recommended.

Step 2

Laboratory Analysis

Blood sample collection via venipuncture.

Step 3

Report Delivery

Sample processed for DNA extraction and NGS analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor and provide detailed clinical history.
2
During the Test:A blood sample will be collected for DNA analysis.
3
After the Test:Results will be available in 3-4 weeks; follow-up with a healthcare provider is recommended.

About This Test

Who Should Get This Test

To diagnose Primary Ciliary Dyskinesia Type 26 by identifying mutations in the CFAP298 gene through next-generation sequencing.

How to Prepare

  • Use blood, extracted DNA, or one drop blood on FTA card.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the CFAP298 gene.
Positive: Pathogenic variant detected, confirming PCD type 26.
Negative: No pathogenic variant detected, but clinical correlation is advised.
Variant of uncertain significance: Further testing or family studies may be needed.
⚠️ When to Consult a Doctor:

If symptoms of PCD are present, or for family planning and genetic counseling.

Risks & Considerations

  • ●Minor bruising at the puncture site
  • ●Rare risk of infection

Frequently Asked Questions

What is CFAP298 Gene Primary Ciliary Dyskinesia Type 26?
It is a rare genetic disorder caused by mutations in the CFAP298 gene, leading to defective cilia function and symptoms like chronic respiratory infections.
How is the NGS Genetic Test performed?
The test uses next-generation sequencing to analyze the DNA sequence of the CFAP298 gene from a blood sample.
What is the cost of the test in India?
The cost is INR 20,000, with free home sample collection available in major cities.
Is home sample collection available?
Yes, free home collection is offered for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What are the symptoms of PCD type 26?
Symptoms include chronic cough, recurrent respiratory infections, difficulty breathing, wheezing, nasal congestion, chronic sinus infections, ear infections, hearing loss, and infertility.
Who should consider this genetic test?
Individuals with symptoms of PCD, a family history of genetic disorders, or those seeking diagnosis for chronic respiratory issues.
What does a positive result mean?
A positive result indicates the presence of a pathogenic variant in the CFAP298 gene, confirming PCD type 26.
Is genetic counseling required?
Genetic counseling is recommended before and after testing to understand the implications and results.
Are there any risks associated with the test?
The test involves a blood draw, which may cause minor bruising or infection risk, but these are minimal.
How accurate is the NGS test?
NGS is a highly accurate method for detecting genetic mutations, but interpretation should be done by a qualified professional.
What should I do after receiving the results?
Consult with a healthcare provider or genetic counselor to discuss the results and plan for management or treatment.
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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For Hospitals & Clinics

Reference 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.

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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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