STAT5B Gene Growth Hormone Insensitivity with Immunodeficiency NGS Genetic DNA Test
Introduction
The STAT5B Gene Growth Hormone Insensitivity with Immunodeficiency NGS Genetic DNA Test is an advanced genetic test designed to identify mutations in the STAT5B gene, which can lead to growth hormone insensitivity and immunodeficiency disorders. Understanding these genetic factors is crucial for effective management and treatment of affected individuals.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect specific mutations in the STAT5B gene. By analyzing the genetic material from blood or extracted DNA, the test provides insights into the genetic basis of growth hormone insensitivity and related immunodeficiency conditions.
Who Should Consider This Test
Individuals exhibiting symptoms such as:
- Short stature or growth delays
- Frequent infections or immune deficiencies
- Family history of growth hormone insensitivity disorders
should consider this test. Additionally, individuals with risk factors related to genetic predispositions may benefit from testing.
Benefits of Taking the Test
- Early identification of genetic disorders
- Informed decision-making regarding treatment options
- Personalized healthcare management
- Family planning and genetic counseling insights
Understanding Your Results
Results from the STAT5B Gene Growth Hormone Insensitivity with Immunodeficiency NGS Genetic DNA Test will be interpreted by qualified genetic counselors or healthcare providers. They will help you understand the implications of the findings and guide you through potential next steps based on your results.
Test Price
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 560000 NGN |
Booking the Test
To take advantage of this essential genetic test, please contact us to book your appointment. You can call or WhatsApp us at +2348077798758. Our team is ready to assist you with any inquiries and guide you through the booking process.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test includes blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected by the STAT5B gene are recommended.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Hepatology Nephrology Endocrinology Disorders
