Aldoa Gene Glycogen Storage Disease Type 12 NGS Genetic DNA Test
Introduction
The Aldoa Gene Glycogen Storage Disease Type 12 NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the Aldoa gene. This gene plays a pivotal role in glycogen metabolism, and its dysfunction can lead to Glycogen Storage Disease Type 12, a rare metabolic disorder. Understanding your genetic predisposition is crucial for early diagnosis and management of this condition.
What the Test Measures
This test specifically measures alterations in the Aldoa gene, which can indicate the presence of Glycogen Storage Disease Type 12. By analyzing the genetic makeup, healthcare providers can identify potential risks and guide treatment options.
Who Should Consider This Test
This test is recommended for individuals who:
- Have a family history of Glycogen Storage Disease Type 12.
- Exhibit symptoms such as muscle weakness, hypoglycemia, or abnormal liver function tests.
- Are at risk due to genetic predisposition.
Consultation with a genetic counselor is advised to discuss personal and family medical history.
Benefits of Taking the Test
- Early detection and diagnosis of Glycogen Storage Disease Type 12.
- Informed decision-making regarding treatment and management options.
- Understanding genetic risks for family members.
- Access to specialized medical care and support.
Understanding Your Results
Results from the Aldoa Gene Glycogen Storage Disease Type 12 NGS Genetic DNA Test will be interpreted by qualified healthcare professionals. They will provide guidance on the implications of the findings and recommend further action if necessary.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
How to Book the Test
To book the Aldoa Gene Glycogen Storage Disease Type 12 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any questions you may have. Don’t wait—take charge of your health today!
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history is essential, along with a genetic counseling session to draw a pedigree chart of family members affected by Glycogen Storage Disease Type 12.
This test falls under the specialty of General Physician and the department of Genetics, focusing on metabolic disorders through NGS technology.
