PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test
Introduction
The PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test is an innovative diagnostic tool that leverages Next-Generation Sequencing (NGS) technology to identify genetic mutations linked to Zellweger syndrome, a serious neurological disorder. This test plays a vital role in early diagnosis, enabling timely interventions and management strategies for affected individuals.
What the Test Measures
This genetic test specifically measures mutations in the PEX16 gene, which are associated with Zellweger syndrome. By analyzing the genetic material from a blood sample or extracted DNA, the test can confirm the presence of these mutations, providing essential information for diagnosis and treatment planning.
Who Should Consider This Test?
Individuals who may benefit from the PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test include:
- Those with a family history of Zellweger syndrome or related neurological disorders.
- Patients exhibiting symptoms such as developmental delays, seizures, or other neurological impairments.
- Individuals seeking genetic counseling to understand their risk of passing on genetic conditions.
Benefits of Taking the Test
Taking the PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test offers numerous benefits:
- Accurate identification of genetic mutations, facilitating early diagnosis.
- Informed decision-making regarding management and treatment options.
- Access to genetic counseling and support for affected families.
- Peace of mind through genetic knowledge and understanding.
Understanding Your Results
Results from the PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test will be communicated to you by our qualified genetic counselors. They will provide guidance on the implications of your results, including any necessary follow-up actions or additional testing that may be required.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Collection and Pre-Test Instructions
Sample collection can be done using:
- Blood
- Extracted DNA
- One drop of blood on an FTA card
Prior to the test, it is essential to have a clinical history of the patient and to attend a genetic counseling session to draw a pedigree chart of family members affected with PEX16 Gene Zellweger syndrome.
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. Don’t wait to gain valuable insights into your genetic health. Book the PEX16 Gene Zellweger Syndrome NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.
