PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 With or Without Anosmia NGS Genetic DNA Test
The PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 With or Without Anosmia NGS Genetic DNA Test is a cutting-edge genetic test that plays a vital role in diagnosing hypogonadotropic hypogonadism, a condition characterized by insufficient hormone production. This test utilizes Next Generation Sequencing (NGS) technology to analyze the PROKR2 gene, which is crucial for reproductive health.
What the Test Measures
This test detects mutations in the PROKR2 gene, which are associated with hypogonadotropic hypogonadism type 3. It helps in understanding the genetic basis of this condition, providing insights into the underlying causes of hormonal imbalances.
Who Should Consider This Test?
- Individuals experiencing delayed puberty or infertility.
- Patients with symptoms of anosmia (loss of smell) along with hormonal issues.
- Those with a family history of hypogonadotropic hypogonadism.
Benefits of Taking the Test
- Accurate diagnosis of genetic causes of hormonal disorders.
- Guidance for targeted treatment options.
- Understanding family risk factors and implications for relatives.
- Informed decision-making regarding reproductive health.
Understanding Your Results
Results from the PROKR2 Gene test will indicate whether there are mutations present in the PROKR2 gene. A genetic counseling session is recommended to help interpret the results and discuss potential next steps.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 NGS Genetic DNA Test | 400,000 | 560,000 |
Book the Test
To book the PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 With or Without Anosmia NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and provide any additional information you may need.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required along with a genetic counseling session to draw a pedigree chart of family members affected by this condition.
Specialties Involved: General Physician, Genetics Department, NGS Technology, and related disorders in Hepatology, Nephrology, and Endocrinology.
