FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test
Introduction to the FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test
The FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test is a specialized genetic test that plays a critical role in diagnosing Kallmann syndrome, a condition characterized by the absence of puberty and a lack of sense of smell (anosmia). This test utilizes Next Generation Sequencing (NGS) technology to analyze the FGFR1 gene, which is known to be associated with this syndrome. Understanding the genetic basis of Kallmann syndrome is essential for effective patient management and family planning.
What the Test Measures
This test specifically measures and detects mutations in the FGFR1 gene. By identifying these genetic alterations, healthcare providers can confirm a diagnosis of Kallmann syndrome and differentiate it from other conditions that may present with similar symptoms.
Who Should Consider This Test?
Individuals who exhibit symptoms such as delayed puberty, anosmia, or a family history of Kallmann syndrome should consider undergoing this genetic test. Additionally, those with risk factors for genetic disorders or abnormalities in sexual development may benefit from this test.
Benefits of Taking the Test
- Provides a definitive diagnosis of Kallmann syndrome.
- Helps in understanding the genetic factors influencing the condition.
- Facilitates informed medical decisions regarding treatment and management.
- Offers insights for family planning and genetic counseling.
- Utilizes advanced NGS technology for accurate results.
Understanding Your Results
Once the test is completed, results will be interpreted by qualified geneticists. A positive result indicates the presence of mutations in the FGFR1 gene, confirming a diagnosis of Kallmann syndrome. On the other hand, a negative result suggests that no mutations were detected, which may lead to further investigation into other potential causes of the symptoms.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the FGFR1 Gene Kallmann Syndrome Type 2 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample required for this test can be blood, extracted DNA, or even a drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to discuss family history and draw a pedigree chart of affected family members.
At DNA Labs Nigeria, we prioritize your health and strive to provide comprehensive genetic testing services to help you understand your genetic makeup and its implications for your health.
