ALG1 Gene Glycosylation Disorder Type 1K Genetic Test
Components: ALG1 Gene Glycosylation Disorder Type 1K 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: Metabolic Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for ALG1 Gene Glycosylation Disorder Type 1K NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation Disorder Type 1K.
Test Details
ALG1 gene glycosylation disorder type 1K NGS genetic test is a genetic test that analyzes the ALG1 gene for mutations or variations that may be associated with glycosylation disorder type 1K. Glycosylation disorders are a group of genetic disorders that affect the process of attaching sugar molecules (glycosylation) to proteins and lipids. These disorders can lead to a wide range of symptoms and complications, including developmental delays, intellectual disabilities, skeletal abnormalities, and organ dysfunction.
The ALG1 gene is responsible for encoding the enzyme alpha-1,2-mannosyltransferase, which is involved in the glycosylation process. Mutations or variations in the ALG1 gene can disrupt the glycosylation process, leading to glycosylation disorder type 1K.
NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the rapid and efficient analysis of multiple genes simultaneously. In the case of ALG1 gene glycosylation disorder type 1K NGS genetic test, NGS technology is used to sequence and analyze the ALG1 gene to identify any mutations or variations that may be present.
This genetic test can be useful for individuals who are suspected to have glycosylation disorder type 1K based on their symptoms and medical history. The test can help confirm the diagnosis and provide valuable information for medical management and genetic counseling.
It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate guidance and counseling based on the results.
| Test Name | ALG1 Gene Glycosylation disorder type 1K 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for ALG1 Gene Glycosylation disorder type 1K NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation disorder type 1K |
| Test Details |
ALG1 gene glycosylation disorder type 1K NGS genetic test is a genetic test that analyzes the ALG1 gene for mutations or variations that may be associated with glycosylation disorder type 1K. Glycosylation disorders are a group of genetic disorders that affect the process of attaching sugar molecules (glycosylation) to proteins and lipids. These disorders can lead to a wide range of symptoms and complications, including developmental delays, intellectual disabilities, skeletal abnormalities, and organ dysfunction. ALG1 gene is responsible for encoding the enzyme alpha-1,2-mannosyltransferase, which is involved in the glycosylation process. Mutations or variations in the ALG1 gene can disrupt the glycosylation process, leading to glycosylation disorder type 1K. NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the rapid and efficient analysis of multiple genes simultaneously. In the case of ALG1 gene glycosylation disorder type 1K NGS genetic test, NGS technology is used to sequence and analyze the ALG1 gene to identify any mutations or variations that may be present. This genetic test can be useful for individuals who are suspected to have glycosylation disorder type 1K based on their symptoms and medical history. The test can help confirm the diagnosis and provide valuable information for medical management and genetic counseling. It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate guidance and counseling based on the results. |
