SLC26A2 Gene Achondrogenesis Type 1B NGS Genetic DNA Test
The SLC26A2 Gene Achondrogenesis Type 1B NGS Genetic DNA Test is an advanced genetic test that plays a pivotal role in diagnosing Achondrogenesis Type 1B, a severe skeletal dysplasia. This condition is characterized by significant growth and developmental challenges due to mutations in the SLC26A2 gene. Understanding the genetic basis of this disorder is essential for effective management and treatment options.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the SLC26A2 gene. By analyzing the DNA, healthcare providers can identify specific genetic alterations that contribute to the development of Achondrogenesis Type 1B.
Who Should Consider This Test?
Individuals with a family history of skeletal dysplasia or those exhibiting symptoms such as disproportionate short stature, joint abnormalities, or other related health issues should consider this test. Additionally, expectant parents with concerns about hereditary conditions may find this test beneficial.
Benefits of Taking the Test
- Early diagnosis leading to timely intervention and management.
- Personalized care plans based on genetic findings.
- Informed reproductive choices for families at risk.
- Access to genetic counseling for better understanding and support.
Understanding Your Results
Upon completion of the test, results will be analyzed and interpreted by genetic specialists. It is crucial to understand that a positive result indicates a mutation in the SLC26A2 gene, which may lead to Achondrogenesis Type 1B. Genetic counseling is recommended to discuss the implications of the results and potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC26A2 Gene Achondrogenesis Type 1B NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today
Don’t wait for symptoms to appear. Take charge of your health by booking the SLC26A2 Gene Achondrogenesis Type 1B NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Turnaround time for results is typically 3 to 4 weeks. Ensure you bring a clinical history of the patient and consider a genetic counseling session to discuss family history relevant to the SLC26A2 gene.
Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
