SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test
Introduction
The SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the SLC25A15 gene, which are responsible for metabolic disorders such as hyperornithinemia, hyperammonemia, and homocitrullinuria. This test employs Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive results, crucial for early diagnosis and management of these conditions.
What the Test Measures
This genetic test measures the presence of specific mutations in the SLC25A15 gene. By analyzing the genetic material, it detects abnormalities that may lead to metabolic disorders, allowing healthcare providers to understand the underlying causes of the patient’s symptoms.
Who Should Consider This Test
Individuals who exhibit symptoms of metabolic disorders, such as:
- Severe neurological symptoms
- Developmental delays
- Elevated ammonia levels in the blood
- Family history of hyperornithinemia or related conditions
should consider undergoing this test to confirm a diagnosis and guide treatment options.
Benefits of Taking the Test
- Early diagnosis of metabolic disorders.
- Informed decision-making regarding treatment and management.
- Identification of at-risk family members.
- Access to genetic counseling for better understanding and support.
Understanding Your Results
Results from the SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test will be provided in a detailed report. If mutations are detected, a genetic counselor will assist in interpreting the results and discussing potential next steps for management and treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking Information
We have branches across Kenya, making it convenient for you to access our services. To book the SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254713408028.
Sample Collection and Instructions
The sample type required for this test can be blood or extracted DNA, or one drop of blood on an FTA card. Before taking the test, it is essential to provide a clinical history and undergo a genetic counseling session to create a pedigree chart of family members affected by hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
Don’t wait any longer; ensure your health and the health of your loved ones by booking the SLC25A15 Gene Hyperornithinemia Hyperammonemia Homocitrullinuria Syndrome NGS Genetic DNA Test today!
