CYBA Gene Granulomatous Disease Chronic Autosomal Recessive Cytochrome B-Negative NGS Genetic DNA Test
Introduction
The CYBA Gene Granulomatous Disease Chronic Autosomal Recessive Cytochrome B-Negative NGS Genetic DNA Test is a specialized genetic test that plays a vital role in diagnosing and understanding granulomatous diseases. This test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the CYBA gene, which can lead to chronic granulomatous disease (CGD). Early diagnosis is essential as it allows for timely management and treatment, significantly improving the quality of life for affected individuals.
What the Test Measures
This genetic test specifically measures mutations in the CYBA gene that are associated with chronic granulomatous disease. It detects whether the genetic material from the individual carries any abnormalities that could predispose them to this condition.
Who Should Consider This Test
- Individuals with a family history of granulomatous disease.
- Patients exhibiting symptoms such as recurrent infections, particularly with catalase-positive organisms.
- Individuals with unexplained granulomatous inflammation.
Benefits of Taking the Test
- Provides clarity on the genetic basis of granulomatous disease.
- Guides treatment options and management strategies.
- Facilitates genetic counseling for family planning.
- Helps in early diagnosis, leading to better health outcomes.
Understanding Your Results
Results from the CYBA Gene test can help healthcare providers understand the genetic predisposition of the patient towards granulomatous diseases. A positive result indicates the presence of mutations that may require further medical intervention and management, while a negative result can provide reassurance.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CYBA Gene Granulomatous Disease Chronic Autosomal Recessive Cytochrome B-Negative NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or even one drop of blood on an FTA card. It is essential to provide a clinical history prior to testing, and a genetic counseling session is recommended to create a pedigree chart of family members affected by the CYBA gene.
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. You can also take advantage of our home sample collection service.
Book Your Test Today!
Don’t wait to get the answers you need. Call or WhatsApp us at +254711564616 to book the CYBA Gene Granulomatous Disease test today!
