SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency NGS Genetic DNA Test
Introduction
The SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency NGS Genetic DNA Test is a revolutionary diagnostic tool that helps identify genetic mutations associated with mitochondrial diseases. These disorders can significantly impact various bodily functions, particularly in the cardiovascular system. Understanding your genetic predisposition can lead to timely interventions and better management of health conditions.
What the Test Measures
This test specifically detects mutations in the SLC25A3 gene, which is responsible for encoding a mitochondrial phosphate carrier. Abnormalities in this gene can lead to phosphate transport issues within mitochondria, affecting energy production and overall cellular function.
Who Should Consider This Test?
Individuals with a family history of mitochondrial diseases, unexplained cardiovascular symptoms, or those experiencing chronic fatigue should consider this test. Symptoms may include:
- Muscle weakness
- Heart-related issues
- Neurological symptoms
- Fatigue
Risk factors include a genetic predisposition to mitochondrial disorders and a family history of similar health issues.
Benefits of Taking the Test
Taking the SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency NGS Genetic DNA Test offers numerous benefits:
- Early detection of genetic predispositions
- Informed decision-making regarding health management
- Guidance for family planning
- Access to personalized treatment options
Understanding Your Results
Results from this test will indicate whether mutations in the SLC25A3 gene are present. A genetic counseling session is recommended to interpret the results accurately and discuss potential implications for health and family members.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t leave your health to chance. Book the SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency NGS Genetic DNA Test today for just 400,000 NGN. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
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 Patient and Genetic Counseling session for pedigree chart creation.
- Specialty: Cardiologist
- Department: Genetics
- Method: NGS Technology
- Disease Type: Cardiovascular Pneumology Disorders