DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test
Introduction to the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test
The DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the DOLK gene, which are associated with glycosylation disorders. These disorders can lead to significant neurological complications, making early detection vital. Utilizing Next Generation Sequencing (NGS) technology, this test provides a comprehensive analysis of the gene, enabling healthcare providers to offer precise diagnoses and tailored treatment plans.
What the Test Measures
This genetic test measures specific alterations in the DOLK gene that may result in glycosylation disorders. By examining the DNA sequence, it detects any mutations that could contribute to neurological issues, helping to identify patients who may benefit from further clinical intervention.
Who Should Consider This Test?
Individuals who exhibit symptoms of neurological disorders or have a family history of glycosylation disorders should consider this test. Common symptoms may include developmental delays, seizures, or other neurological impairments. Additionally, those with risk factors such as a family pedigree chart indicating affected members are encouraged to undergo testing.
Benefits of Taking the Test
- Early identification of potential genetic disorders.
- Guidance for treatment and management options.
- Informed decision-making for family planning.
- Access to specialized care from neurologists and genetic counselors.
Understanding Your Results
Upon receiving your results, it is essential to consult with a healthcare professional who can interpret the findings. Results may indicate whether a genetic mutation is present and what implications this may have for your health. Genetic counseling is recommended to help you understand the next steps and any necessary actions.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to uncover your genetic predisposition to neurological disorders. Book the DOLK Gene Glycosylation Disorder Type 1M NGS Genetic DNA Test today by calling or sending a WhatsApp message to +2348077798758. Take control of your health and ensure a brighter future.
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 is required, along with a genetic counseling session to draw a pedigree chart of family members affected with DOLK Gene Glycosylation Disorder Type 1M.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
