B4GALT1 Gene Glycosylation Disorder Type 2D NGS Genetic DNA Test
Introduction to the Test
The B4GALT1 Gene Glycosylation Disorder Type 2D NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the B4GALT1 gene. This gene plays a vital role in the glycosylation process, which is crucial for proper cellular function. Disorders related to glycosylation can lead to various neurological complications, making early diagnosis and intervention imperative.
What the Test Measures
This genetic test measures the presence of specific mutations in the B4GALT1 gene, which can indicate a predisposition to glycosylation disorders. By analyzing the genetic makeup, healthcare providers can better understand the underlying causes of neurological symptoms.
Who Should Consider This Test?
Individuals experiencing neurological symptoms such as developmental delays, cognitive impairments, or unexplained neurological disorders should consider this test. Additionally, those with a family history of glycosylation disorders or related conditions may also benefit from this genetic evaluation.
Benefits of Taking the Test
- Early detection of potential genetic disorders.
- Informed decision-making regarding treatment and management.
- Understanding of familial risk factors for genetic conditions.
- Access to genetic counseling and support services.
Understanding Your Results
Results from the B4GALT1 Gene Glycosylation Disorder Type 2D NGS Genetic DNA Test can provide insight into potential genetic mutations. A healthcare provider will discuss the findings with you, helping you understand what they mean for your health and any necessary next steps.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| B4GALT1 Gene Glycosylation Disorder Type 2D NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the B4GALT1 Gene Glycosylation Disorder Type 2D NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: It is essential to have a clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with B4GALT1 Gene Glycosylation Disorder Type 2D.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
