MRPL3 Gene Combined Oxidative Phosphorylation Deficiency Type 9 NGS Genetic DNA Test
Introduction
The MRPL3 Gene Combined Oxidative Phosphorylation Deficiency Type 9 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with metabolic disorders, specifically those affecting mitochondrial function. By utilizing Next-Generation Sequencing (NGS) technology, this test provides an in-depth analysis of the MRPL3 gene, which plays a vital role in mitochondrial protein synthesis.
What the Test Measures
This test measures the presence of mutations in the MRPL3 gene that can lead to combined oxidative phosphorylation deficiency. It helps detect abnormalities that may contribute to various metabolic disorders, providing valuable insights into an individual’s genetic health.
Who Should Consider This Test
Individuals exhibiting symptoms of metabolic disorders, such as:
- Unexplained muscle weakness
- Neurological issues
- Developmental delays in children
- Fatigue and exercise intolerance
Additionally, those with a family history of metabolic disorders or mitochondrial diseases should consider this test to understand their risk factors better.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions affecting mitochondrial function.
- Informed decision-making regarding treatment and management options.
- Potential for early intervention in at-risk individuals.
- Understanding hereditary patterns that may affect family members.
Understanding Your Results
Results from the MRPL3 Gene Combined Oxidative Phosphorylation Deficiency Type 9 NGS Genetic DNA Test will be provided in a comprehensive report. It is essential to consult with a healthcare provider or genetic counselor to interpret the results accurately and discuss potential implications for health and family planning.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu, making it convenient for you to access our services. To book the MRPL3 Gene Combined Oxidative Phosphorylation Deficiency Type 9 NGS Genetic DNA Test, contact us at +254711564616 or visit our website to schedule an appointment.
Turnaround Time and Sample Type
The test has a turnaround time of 3 to 4 weeks. The sample required can be:
- Blood
- Extracted DNA
- One drop of blood on FTA Card
Pre-Test Instructions
Before undergoing the MRPL3 Gene Combined Oxidative Phosphorylation Deficiency Type 9 NGS Genetic DNA Test, it is essential to have a clinical history review and a genetic counseling session. This will involve drawing a pedigree chart of family members affected by combined oxidative phosphorylation deficiency type 9 to better understand the genetic implications.
Take the first step towards understanding your genetic health today!
