AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test
Introduction
The AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the AMPD2 gene, which are associated with pontocerebellar hypoplasia, a rare neurological disorder. This test utilizes Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive results, aiding in the diagnosis and management of this condition.
What the Test Measures
This test specifically measures genetic variations in the AMPD2 gene, which can lead to developmental issues in the brain, particularly affecting the cerebellum and pons. By detecting these mutations, healthcare providers can offer tailored treatment options and support.
Who Should Consider This Test
Individuals who may benefit from the AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test include:
- Patients exhibiting symptoms of neurological disorders, such as developmental delays, motor dysfunction, or coordination difficulties.
- Families with a history of pontocerebellar hypoplasia or related genetic conditions.
- Individuals seeking genetic counseling for family planning purposes.
Benefits of Taking the Test
Taking the AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of genetic conditions, enabling informed medical decisions.
- Understanding of the genetic basis of the disorder, which can guide treatment options.
- Support for affected families through genetic counseling and resources.
- Potential for early intervention and management strategies to improve patient outcomes.
Understanding Your Results
Results from the AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test will be provided with a detailed report explaining any detected mutations. It is essential to consult with a healthcare professional or genetic counselor to interpret the results accurately and discuss potential implications for health and family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical history of the patient going for the test and a genetic counseling session to draw a pedigree chart of family members affected with AMPD2 Gene Pontocerebellar hypoplasia.
Contact Us
We have branches across Kenya, making it convenient for you to access our services. To book the AMPD2 Gene Pontocerebellar Hypoplasia Type 9 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Ensure you take a proactive step towards understanding your health today!
