IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 NGS Genetic DNA Test
Introduction
The IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic predispositions to mitochondrial dysfunctions associated with neurological disorders. Mitochondrial dysfunction can lead to a variety of health issues, making early detection crucial for effective management and treatment.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the IBA57 gene. It detects mutations that may contribute to mitochondrial dysfunctions, providing valuable insights into the underlying genetic causes of neurological disorders.
Who Should Consider This Test
Individuals with a family history of mitochondrial disorders, neurological symptoms such as muscle weakness, seizures, or developmental delays, and those with unexplained medical conditions should consider this test. It is particularly beneficial for patients experiencing:
- Unexplained neurological symptoms
- Muscle weakness or pain
- Developmental delays in children
- Seizures without a known cause
Benefits of Taking the Test
- Early identification of genetic predispositions to mitochondrial dysfunctions.
- Informed decision-making regarding treatment and management strategies.
- Personalized care plans tailored to the patient’s genetic profile.
- Support for family planning and genetic counseling.
Understanding Your Results
Results from the IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or medical professional. They will provide guidance on the implications of the findings and discuss potential next steps.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To ensure you receive the best care, we recommend a clinical history review and a genetic counseling session to draw a pedigree chart of family members affected by IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3. Book your test today by calling or WhatsApp us at +2348077798758. Our team is here to assist you with any questions and guide you through the testing process.
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
