AMPD1 Gene Myopathy Due to Myoadenylate Deaminase Deficiency NGS Genetic DNA Test
Introduction
The AMPD1 Gene Myopathy due to myoadenylate deaminase deficiency NGS Genetic DNA Test is a vital diagnostic tool used to identify genetic mutations associated with metabolic disorders. This test utilizes Next-Generation Sequencing (NGS) technology, allowing for a comprehensive analysis of the AMPD1 gene. Understanding your genetic predisposition can lead to early interventions and better management of related health conditions.
What the Test Measures
This genetic test detects mutations in the AMPD1 gene, which is responsible for encoding the enzyme myoadenylate deaminase. This enzyme plays a crucial role in energy metabolism within muscle tissues. Deficiencies or mutations can lead to myopathy, characterized by muscle weakness and exercise intolerance.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Muscle weakness
- Exercise intolerance
- Cramping or fatigue during physical activities
Additionally, those with a family history of metabolic disorders or myopathy should consider this test to assess their genetic risk factors.
Benefits of Taking the Test
- Early diagnosis of potential metabolic disorders
- Informed decision-making regarding lifestyle and treatment options
- Access to genetic counseling and support services
- Increased understanding of personal and family health risks
Understanding Your Results
Results from the AMPD1 Gene Myopathy test will indicate whether mutations are present. A genetic counselor will assist in interpreting these results, providing guidance on the implications for your health and that of your family. Understanding your results is crucial for making informed health decisions.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To schedule your AMPD1 Gene Myopathy due to myoadenylate deaminase deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in understanding your genetic health and taking proactive steps towards wellness.
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 is required. A genetic counseling session to draw a pedigree chart of family members affected with myopathy due to myoadenylate deaminase deficiency is recommended.
Specialties: General Physician, Genetics Department, NGS Technology, Metabolic Disorders.
