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ARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic Test

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ARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic Test

Short Name: ARMC4 PCD Type 23 NGS Test

Also known as: PCD Type 23 Genetic Test, ARMC4 Mutation Analysis

ARMC4 Gene Primary ciliary dyskinesia type 23 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.

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 detect mutations in the ARMC4 gene for definitive diagnosis of primary ciliary dyskinesia type 23, aiding in early intervention, symptom management, and genetic counseling.

Test Code
4777
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)
Step 1

Sample Collection

No special preparation required. Inform the healthcare provider about any medications or medical history.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm using standard venipuncture techniques.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor to understand the test implications and provide informed consent.
2
During the Test:Sample collection followed by DNA extraction and NGS analysis in the laboratory.
3
After the Test:Review results with a healthcare provider to discuss diagnosis, management options, and family implications.

About This Test

Who Should Get This Test

To detect mutations in the ARMC4 gene for definitive diagnosis of primary ciliary dyskinesia type 23, aiding in early intervention, symptom management, and genetic counseling.

How to Prepare

  • Avoid strenuous activity before sample collection
  • Ensure proper identification and labeling of the sample

Doctor's Notes

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

"Early genetic testing for PCD type 23 can guide treatment, improve respiratory health, and inform family planning decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood
ContainerEDTA tube
Collection MethodVenipuncture

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the ARMC4 gene, which are associated with primary ciliary dyskinesia type 23.
📊

Positive

Pathogenic variant detected in ARMC4 gene, consistent with PCD type 23. Clinical correlation and genetic counseling recommended.

📊

Negative

No pathogenic variants detected in ARMC4 gene. PCD type 23 is unlikely, but other causes may be considered.

📊

Variant of uncertain significance

A genetic variant was found but its clinical significance is unclear. Further testing and family studies may be needed.

⚠️ When to Consult a Doctor:

If symptoms such as chronic cough or recurrent infections persist, or if there is a family history of PCD, consult a pulmonologist or genetic specialist.

Limitations

  • ⚠May not detect all genetic variants or non-ARMC4 related PCD
  • ⚠Requires integration with clinical evaluation and other diagnostic tests

Risks & Considerations

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

Interfering Factors

  • ●Contaminated or degraded DNA sample
  • ●Recent blood transfusion

Compare With Similar Tests

TestARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic TestHigh-speed video microscopyNasal nitric oxide measurementOther gene panels for PCD
ComparisonARMC4 Gene Primary ciliary dyskinesia type 23 NGS Genetic Test

Frequently Asked Questions

What is primary ciliary dyskinesia type 23?
PCD type 23 is a rare genetic disorder caused by mutations in the ARMC4 gene, leading to dysfunctional cilia and respiratory issues.
How is the ARMC4 gene test performed?
The test uses next-generation sequencing (NGS) to analyze DNA from a blood sample for mutations in the ARMC4 gene.
What is the cost of the ARMC4 Gene PCD Type 23 NGS Test?
The test costs INR 20000, with home sample collection available across India.
Who should consider this genetic test?
Individuals with symptoms like chronic cough, recurrent infections, or a family history of PCD should consider testing.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
What do the test results mean?
Results indicate if pathogenic mutations are present in the ARMC4 gene, aiding in diagnosis of PCD type 23.
Are there any risks associated with the test?
The test involves minimal risks from blood draw, such as bruising, and potential psychological impact of genetic findings.
Can this test detect all types of PCD?
No, this test specifically targets the ARMC4 gene for PCD type 23. Other genes may require separate testing.
Is genetic counseling recommended?
Yes, genetic counseling is advised to interpret results and understand implications for family planning.
What should I do if I test positive?
Consult a healthcare provider for management options, which may include respiratory therapies and regular monitoring.
Is the test covered by insurance?
Coverage varies; check with your insurance provider or schemes like PMJAY for details.
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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