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NME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

NME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic Test

Short Name: NME8 Gene PCD Type 6 NGS Test

Also known as: Primary Ciliary Dyskinesia Type 6, PCD Type 6, NME8 Gene Mutation Test

NME8 Gene Primary ciliary dyskinesia type 6 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 TestAll Ages🏠 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 6 by identifying mutations in the NME8 gene using NGS technology, enabling early intervention and genetic counseling.

Test Code
4786
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

No specific preparation required. Provide detailed clinical history and family pedigree.

Method: Blood Collection

Step 2

Laboratory Analysis

Blood sample will be collected by a trained phlebotomist using sterile techniques.

Step 3

Report Delivery

Apply pressure to the puncture site. Sample will be processed and stored appropriately for analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Provide detailed clinical history, family pedigree, and informed consent for genetic testing.
2
During the Test:Sample collection, DNA extraction, and NGS analysis performed in a certified laboratory.
3
After the Test:Report generation, genetic counseling session, and discussion of results with healthcare provider.

About This Test

Who Should Get This Test

To diagnose Primary Ciliary Dyskinesia Type 6 by identifying mutations in the NME8 gene using NGS technology, enabling early intervention and genetic counseling.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection equipment
  • Label samples correctly with patient details

Doctor's Notes

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

"Early genetic testing for PCD Type 6 can guide management, family planning, and improve patient outcomes through targeted interventions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Incorrect labeling or documentation

Understanding Your Results

Results indicate the presence or absence of mutations in the NME8 gene associated with Primary Ciliary Dyskinesia Type 6.
📊

Positive for pathogenic variant

Confirms diagnosis of PCD Type 6. Genetic counseling and management planning recommended.

📊

Negative

No pathogenic variants detected. Clinical correlation and further testing may be advised if symptoms persist.

📊

Variant of uncertain significance

Further family studies or functional assays may be needed for clarification.

⚠️ When to Consult a Doctor:

If symptoms such as chronic cough, sinus infections, or infertility persist, or if there is a family history of PCD, consult a geneticist or pulmonologist for evaluation.

Limitations

  • ⚠May not detect all genetic variants
  • ⚠Requires genetic counseling for interpretation
  • ⚠Results may have variants of uncertain significance

Risks & Considerations

  • ●Minimal risk from blood draw (e.g., bruising, infection)
  • ●Psychological impact of genetic results
  • ●Potential for incidental findings

Interfering Factors

  • ●Poor sample quality
  • ●Contamination during collection
  • ●Insufficient DNA quantity

Compare With Similar Tests

TestNME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic Test
ComparisonNME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic Test

Frequently Asked Questions

What is NME8 Gene PCD Type 6?
It is a rare genetic disorder caused by mutations in the NME8 gene, leading to impaired ciliary function and respiratory issues.
What are the symptoms of PCD Type 6?
Symptoms include chronic cough, recurrent sinus infections, bronchiectasis, hearing loss, dizziness, infertility, and situs inversus.
How is PCD Type 6 diagnosed?
Diagnosis involves clinical evaluation, imaging tests, and genetic testing such as NGS to detect NME8 gene mutations.
What is NGS Genetic Testing?
Next-Generation Sequencing (NGS) is an advanced technology that analyzes multiple genes simultaneously for comprehensive genetic analysis.
What is the cost of the NME8 Gene PCD Type 6 NGS Test?
The test costs INR 20000.0, with free home sample collection available across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result confirms the presence of pathogenic variants in the NME8 gene, indicating PCD Type 6. Genetic counseling is recommended.
Can PCD Type 6 be treated?
While there is no cure, management focuses on symptom relief, such as airway clearance therapies and antibiotics for infections.
Is genetic counseling provided?
Yes, genetic counseling is included to help interpret results and discuss implications for family planning.
What samples are required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card can be used for sample collection.
Is the test available in my city?
The test is available in major cities across India, including Mumbai, Delhi, Bangalore, and many more, with home collection services.
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.

LIMS Integration

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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