Acy1 Gene Aminoacylase Deficiency NGS Genetic DNA Test
Introduction
The Acy1 Gene Aminoacylase Deficiency NGS Genetic DNA Test is a vital diagnostic tool designed to identify genetic mutations associated with aminoacylase deficiency. This condition can lead to various metabolic disorders, affecting the body’s ability to process amino acids effectively. Understanding your genetic predisposition through this test can significantly impact your health management and treatment options.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the ACY1 gene. These mutations can lead to aminoacylase deficiency, which may result in a range of metabolic disorders. By identifying these genetic variations, healthcare providers can offer tailored treatment plans.
Who Should Consider This Test?
Individuals who exhibit symptoms of metabolic disorders or have a family history of aminoacylase deficiency should consider this test. Common symptoms include:
- Unexplained metabolic issues
- Neurological symptoms
- Developmental delays in children
- Recurrent infections
Additionally, those with risk factors such as a family history of genetic disorders are encouraged to undergo testing.
Benefits of Taking the Test
- Early detection of genetic disorders
- Informed decision-making regarding health management
- Personalized treatment options based on genetic findings
- Better understanding of familial health risks
Understanding Your Results
Results from the Acy1 Gene Aminoacylase Deficiency NGS Genetic DNA Test will provide insights into any identified mutations. A healthcare professional will guide you through the results, helping you understand their implications for your health and any necessary steps moving forward.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Acy1 Gene Aminoacylase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Your Test
To book the Acy1 Gene Aminoacylase Deficiency NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you in scheduling your test and providing any additional information you may need.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counselling session to draw a pedigree chart of family members affected by aminoacylase deficiency.
Don’t wait to take control of your health. Book your test today!
