CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test
Introduction to the Test
The CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with Kallmann syndrome, a condition characterized by the absence of the sense of smell (anosmia) and hypogonadotropic hypogonadism. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive analysis of the CHD7 gene.
What the Test Measures
This genetic test specifically measures alterations in the CHD7 gene, which plays a crucial role in the development of the hypothalamus and olfactory system. By detecting mutations in this gene, healthcare providers can better understand the underlying causes of Kallmann syndrome in patients.
Who Should Consider This Test?
This test is particularly recommended for individuals experiencing:
- Delayed or absent puberty
- Loss of sense of smell
- Family history of Kallmann syndrome or related conditions
- Symptoms of hormone deficiencies
Benefits of Taking the Test
Taking the CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of genetic causes of Kallmann syndrome.
- Informed decision-making regarding treatment options.
- Understanding of hereditary patterns in families.
- Access to genetic counseling for better management of symptoms.
Understanding Your Results
Results from the CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test will be interpreted by genetic specialists. They will provide guidance on the implications of the findings and recommend further steps, which may include treatment options or additional testing.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the CHD7 Gene Kallmann Syndrome Type 5 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and providing any additional information you may need.
Additional Information
Turnaround time for test results is approximately 3 to 4 weeks. The sample type required for this test includes blood or extracted DNA, or one drop of blood on an FTA card. Prior to the test, a genetic counseling session is recommended to discuss the clinical history and draw a pedigree chart of affected family members.
For more information about our services and to understand the importance of genetic testing in pediatrics and dysmorphology, feel free to reach out to us. Your health is our priority!
