DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test
Introduction
The DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test is a sophisticated diagnostic tool that aids in identifying metabolic disorders linked to glycosylation anomalies. Glycosylation is a critical biochemical process, and disruptions can lead to severe health issues. This test is essential for individuals with a family history of glycosylation disorders, allowing for early diagnosis and effective management.
What the Test Measures
This test specifically analyzes the DOLK gene, which is responsible for proper glycosylation. It utilizes Next-Generation Sequencing (NGS) technology to detect mutations or variations in the gene that may contribute to metabolic disorders.
Who Should Consider This Test
Individuals who should consider the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test include:
- Those with a family history of glycosylation disorders.
- Patients exhibiting symptoms of metabolic disorders such as developmental delays, neurological issues, or unexplained health problems.
- Individuals seeking genetic counseling for informed family planning.
Benefits of Taking the Test
- Early detection of potential metabolic disorders.
- Informed decision-making regarding health management and family planning.
- Access to tailored treatment options based on genetic findings.
- Peace of mind through understanding genetic risks.
Understanding Your Results
Results from the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test will provide insights into your genetic predispositions. A genetic counselor will assist in interpreting the results, discussing implications, and suggesting possible next steps for management or treatment.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To schedule your DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to book online. Our team is here to assist you in understanding your genetic health and ensuring you receive the best care possible.
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 and a genetic counseling session to draw a pedigree chart of family members affected with Glycosylation disorder type 1M.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
