SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test
The SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test is a cutting-edge genetic test that plays a pivotal role in diagnosing and understanding glycosylation disorders, particularly those affecting the neurological system. This test is essential for individuals who may be at risk of developing conditions linked to the SLC35C1 gene, which is crucial for proper glycosylation processes in the body.
What the Test Measures
This genetic test detects mutations in the SLC35C1 gene, which can lead to glycosylation disorders. These disorders are characterized by the improper addition of sugar molecules to proteins and lipids, affecting numerous bodily functions, particularly in the nervous system.
Who Should Consider This Test
Individuals with a family history of neurological disorders or those exhibiting symptoms such as developmental delays, intellectual disabilities, or other neurological symptoms should consider this test. It is also recommended for patients referred by a neurologist for genetic evaluation.
Benefits of Taking the Test
- Accurate diagnosis of glycosylation disorders.
- Informed decision-making regarding treatment options.
- Understanding the risk of passing on genetic conditions to offspring.
- Access to tailored medical care and support services.
Understanding Your Results
Results from the SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test will provide insights into the presence of mutations. A genetic counseling session is recommended to help interpret the results and discuss potential implications for health and family planning.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book Your Test Today
To schedule your SLC35C1 Gene Glycosylation Disorder Type 2C NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in taking this important step towards understanding your genetic health.
Additional Information
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 is required along with a genetic counseling session to draw a pedigree chart of family members affected with SLC35C1 Gene Glycosylation Disorder Type 2C.
This test is conducted using NGS technology and is crucial for patients under the care of a neurologist in the Genetics department. Gain insights into your genetic health today!
