SLC35A1 Gene Glycosylation disorder type 2F Genetic Test
Components: SLC35A1 Gene Glycosylation disorder type 2F Genetic Test
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC35A1 Gene Glycosylation disorder type 2F.
Test Details
The SLC35A1 gene is associated with glycosylation disorder type 2F, also known as congenital disorder of glycosylation type 2F (CDG2F). This genetic disorder affects the body’s ability to produce and attach sugar molecules to proteins, which can cause a wide range of symptoms including developmental delays, intellectual disability, seizures, and abnormal facial features.
NGS (next-generation sequencing) genetic testing is a type of DNA testing that can analyze multiple genes at once, quickly and accurately. A NGS genetic test for the SLC35A1 gene can identify any variations or mutations in the gene that may be causing CDG2F. This information can help healthcare providers diagnose the disorder and provide appropriate treatment and management strategies for affected individuals.
Test Name | SLC35A1 Gene Glycosylation disorder type 2F Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for SLC35A1 Gene Glycosylation disorder type 2F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SLC35A1 Gene Glycosylation disorder type 2F |
Test Details |
The SLC35A1 gene is associated with glycosylation disorder type 2F, also known as congenital disorder of glycosylation type 2F (CDG2F). This genetic disorder affects the body’s ability to produce and attach sugar molecules to proteins, which can cause a wide range of symptoms including developmental delays, intellectual disability, seizures, and abnormal facial features. NGS (next-generation sequencing) genetic testing is a type of DNA testing that can analyze multiple genes at once, quickly and accurately. A NGS genetic test for the SLC35A1 gene can identify any variations or mutations in the gene that may be causing CDG2F. This information can help healthcare providers diagnose the disorder and provide appropriate treatment and management strategies for affected individuals. |