ATP5F1A Gene Combined Oxidative Phosphorylation Deficiency Type 22 NGS Genetic DNA Test
Introduction
The ATP5F1A Gene Combined Oxidative Phosphorylation Deficiency Type 22 NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify potential genetic mutations associated with mitochondrial disorders. This test plays a vital role in understanding the genetic basis of metabolic disorders, enabling healthcare providers to offer tailored treatment options for affected individuals.
What the Test Measures
This genetic test focuses on detecting mutations in the ATP5F1A gene, which is crucial for mitochondrial function. By utilizing Next-Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the gene, allowing for the identification of any abnormalities that may lead to oxidative phosphorylation deficiencies.
Who Should Consider This Test
Individuals who exhibit symptoms related to metabolic disorders, such as unexplained muscle weakness, neurological issues, or developmental delays, should consider this test. Additionally, those with a family history of mitochondrial disorders or who are at risk due to genetic factors may benefit from this testing.
Benefits of Taking the Test
- Early identification of potential genetic disorders.
- Informed decision-making regarding treatment options.
- Understanding the hereditary nature of the disorder.
- Access to genetic counseling for family planning.
Understanding Your Results
Results from the ATP5F1A Gene Combined Oxidative Phosphorylation Deficiency Type 22 NGS Genetic DNA Test will provide insights into the presence of mutations. A healthcare professional will help interpret these results, discussing their implications for health and any necessary follow-up actions.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| ATP5F1A Gene Combined Oxidative Phosphorylation Deficiency Type 22 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To take the first step towards understanding your genetic health, book the ATP5F1A Gene Combined Oxidative Phosphorylation Deficiency Type 22 NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
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 of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Combined Oxidative Phosphorylation Deficiency Type 22.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
