SEMA3A Gene Kallmann Syndrome SEMA3A Related NGS Genetic DNA Test
Introduction
The SEMA3A Gene Kallmann Syndrome SEMA3A Related NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Kallmann syndrome. This condition is characterized by delayed puberty and a loss of the sense of smell (anosmia). Understanding your genetic predisposition is crucial for effective management and treatment options.
What the Test Measures
This test measures mutations in the SEMA3A gene, which plays a significant role in the development of the reproductive system. By utilizing Next-Generation Sequencing (NGS) technology, we can detect variations that may lead to Kallmann syndrome.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Delayed puberty
- Anosmia (loss of smell)
- Family history of Kallmann syndrome or related genetic disorders
should consider this test. Risk factors include male gender and a family history of reproductive or olfactory disorders.
Benefits of Taking the Test
- Early diagnosis of Kallmann syndrome, leading to timely intervention.
- Provides valuable information for family planning and genetic counseling.
- Helps in understanding the underlying causes of symptoms.
- Guides treatment options and management strategies.
Understanding Your Results
Results from the SEMA3A Gene Kallmann Syndrome test will be interpreted by our qualified genetic counselors. They will provide insights into what the results mean for your health and any necessary follow-up actions.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 40,000 KSh | 56,000 KSh |
Book Your Test Today!
We have branches across Kenya, and we also provide home sample collection services for your convenience. Don’t wait to understand your genetic health—book the SEMA3A Gene Kallmann Syndrome SEMA3A Related NGS Genetic DNA Test today!
For more information or to schedule your appointment, call or WhatsApp us at +254711564616.
