GLDC Gene Glycine Encephalopathy Genetic Test
Cost: AED 4400.0
Components:
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Hepatology Nephrology Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for GLDC Gene Glycine encephalopathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GLDC Gene Glycine encephalopathy NGS Genetic DNA Test gene GLDC.
Test Details:
GLDC gene glycine encephalopathy NGS genetic test is a type of genetic test that analyzes the GLDC gene for mutations associated with glycine encephalopathy. Glycine encephalopathy is a rare genetic disorder characterized by the accumulation of glycine, an amino acid, in the brain and other organs.
The GLDC gene provides instructions for making an enzyme called glycine decarboxylase, which is responsible for breaking down glycine. Mutations in the GLDC gene can lead to a decrease or complete loss of enzyme activity, resulting in the accumulation of glycine in the body.
The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of genetic variations. By identifying mutations in the GLDC gene, this test can confirm a diagnosis of glycine encephalopathy and help guide treatment and management options.
It is important to note that this genetic test should be interpreted by a healthcare professional or genetic counselor who specializes in genetics, as the results may have implications for the individual and their family members.
| Test Name | GLDC Gene Glycine encephalopathy Genetic Test |
|---|---|
| Components | |
| 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for GLDC Gene Glycine encephalopathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GLDC Gene Glycine encephalopathy NGS Genetic DNA Test gene GLDC |
| Test Details | GLDC gene glycine encephalopathy NGS genetic test is a type of genetic test that analyzes the GLDC gene for mutations associated with glycine encephalopathy. Glycine encephalopathy is a rare genetic disorder characterized by the accumulation of glycine, an amino acid, in the brain and other organs. The GLDC gene provides instructions for making an enzyme called glycine decarboxylase, which is responsible for breaking down glycine. Mutations in the GLDC gene can lead to a decrease or complete loss of enzyme activity, resulting in the accumulation of glycine in the body. The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of genetic variations. By identifying mutations in the GLDC gene, this test can confirm a diagnosis of glycine encephalopathy and help guide treatment and management options. It is important to note that this genetic test should be interpreted by a healthcare professional or genetic counselor who specializes in genetics, as the results may have implications for the individual and their family members. |
