UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 NGS Genetic DNA Test
Introduction
The UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the UQCC2 gene, which are linked to mitochondrial complex III deficiency. This condition can lead to various neurological disorders, making early detection crucial for effective management and treatment.
What the Test Measures
This test employs Next-Generation Sequencing (NGS) technology to accurately detect genetic mutations in the UQCC2 gene. By analyzing the DNA, it helps determine if a patient has inherited or developed a mutation that could lead to mitochondrial dysfunction.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Neurological disorders
- Muscle weakness
- Seizures
- Developmental delays
Additionally, those with a family history of mitochondrial disorders or neurological conditions may benefit from this test.
Benefits of Taking the Test
- Accurate diagnosis of mitochondrial disorders
- Informed treatment decisions
- Guidance for family planning and genetic counseling
- Access to specialized care and support
Understanding Your Results
Results from the UQCC2 Gene Mitochondrial Complex III Deficiency Test will be provided along with a comprehensive interpretation by our genetic specialists. This guidance will help you understand the implications of your results and the next steps in your healthcare journey.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking Information
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu. To book the UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 NGS Genetic DNA Test, please call or WhatsApp us at +254713408028. Our team is ready to assist you with scheduling your test and answering any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history is required along with a genetic counseling session to draw a pedigree chart of affected family members.
This test is particularly relevant for patients under the care of a neurologist and falls under the genetics specialty, focusing on neurological disorders. With the UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 NGS Genetic DNA Test, you can take a proactive step in understanding your health.
