NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test
Introduction
The NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test is a specialized genetic diagnostic tool that plays a pivotal role in identifying individuals at risk of Nijmegen Breakage Syndrome (NBS), a rare genetic disorder. This test employs Next-Generation Sequencing (NGS) technology to analyze the NBN gene, which is crucial for maintaining genomic stability. Understanding your genetic predisposition can help in early intervention and management of potential health issues.
What the Test Measures
This test specifically measures variations in the NBN gene that are associated with Nijmegen Breakage Syndrome. By identifying these genetic mutations, healthcare providers can assess the risk of developing related health complications, enabling proactive care.
Who Should Consider This Test
Individuals who may benefit from the NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test include:
- Those with a family history of Nijmegen Breakage Syndrome or related dysmorphology disorders.
- Patients exhibiting symptoms such as immunodeficiency, growth retardation, or developmental delays.
- Individuals seeking genetic counseling to understand their risks and family planning options.
Benefits of Taking the Test
Undergoing the NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test offers several benefits:
- Early identification of genetic predispositions, allowing for timely medical intervention.
- Informed family planning decisions based on genetic information.
- Access to specialized care and support for affected individuals and families.
Understanding Your Results
Once the test is completed, results will be provided within 3 to 4 weeks. A genetic counselor will assist in interpreting the results, explaining any identified mutations in the NBN gene and their implications for your health and that of your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Collection and Pre-Test Instructions
The sample type required for this test includes blood, extracted DNA, or one drop of blood on an FTA card. It is essential to have a clinical history of the patient and to undergo a genetic counseling session to draw a pedigree chart of family members affected by the NBN Gene.
Branches and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu. Our dedicated team is here to assist you with the NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test. To book your test or for more information, please call or WhatsApp us at +254711564616.
