BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test
Introduction
The BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze the BCHE gene, which is crucial for the metabolism of certain drugs and chemicals in the body. This test is particularly important for individuals who may have a genetic predisposition to Butyrylcholinesterase deficiency, a condition that can lead to adverse reactions to anesthesia and other medications.
What the Test Measures
This genetic test measures variations in the BCHE gene that may affect the production and function of the butyrylcholinesterase enzyme. By identifying these genetic variations, healthcare providers can assess a patient’s risk for developing complications related to Butyrylcholinesterase deficiency.
Who Should Consider This Test
Individuals who should consider the BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test include:
- Patients with a family history of adverse reactions to anesthetics or certain medications.
- Individuals experiencing unexplained sensitivity to drugs.
- Those with a clinical history suggesting metabolic disorders.
Benefits of Taking the Test
The benefits of undergoing the BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test include:
- Early identification of genetic predispositions to metabolic disorders.
- Informed decisions regarding medication and anesthesia use.
- Personalized healthcare plans based on genetic risk factors.
- Peace of mind for patients and their families.
Understanding Your Results
After the test, results will be provided to you along with guidance on what they mean. A genetic counselor will help interpret the findings and discuss any necessary next steps or treatment options. It is essential to understand that a positive result does not guarantee the development of the deficiency but indicates a higher risk.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
How to Book the Test
To book the BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and providing any additional information you may need.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient who is going for the test and a genetic counseling session to draw a pedigree chart of family members affected with Butyrylcholinesterase deficiency.
Explore the importance of understanding your genetic health with the BCHE Gene Butyrylcholinesterase Deficiency NGS Genetic DNA Test. Book your test today!
