DNAJC19 Gene 3-methylglutaconic aciduria type 5 Genetic Test
Components: DNAJC19 Gene 3-methylglutaconic aciduria type 5 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 DNAJC19 Gene 3-methylglutaconic aciduria type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with 3-methylglutaconic aciduria type 5.
Test Details
The DNAJC19 gene is associated with a condition called 3-methylglutaconic aciduria type 5. This is a rare genetic disorder characterized by an accumulation of 3-methylglutaconic acid in the body, leading to various symptoms such as developmental delay, movement disorders, muscle weakness, and intellectual disability.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. It uses advanced sequencing technology to examine the DNA sequence of the genes of interest. In the case of 3-methylglutaconic aciduria type 5, NGS genetic testing can be used to identify mutations or variations in the DNAJC19 gene that may be responsible for the condition.
NGS genetic testing can help in the diagnosis of 3-methylglutaconic aciduria type 5 by detecting specific genetic changes in the DNAJC19 gene. This information can be used to confirm the diagnosis, provide genetic counseling, and guide treatment decisions.
It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the results.
| Test Name | DNAJC19 Gene 3-methylglutaconic aciduria type 5 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 DNAJC19 Gene 3-methylglutaconic aciduria type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 3-methylglutaconic aciduria type 5 |
| Test Details |
The DNAJC19 gene is associated with a condition called 3-methylglutaconic aciduria type 5. This is a rare genetic disorder characterized by an accumulation of 3-methylglutaconic acid in the body, leading to various symptoms such as developmental delay, movement disorders, muscle weakness, and intellectual disability. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. It uses advanced sequencing technology to examine the DNA sequence of the genes of interest. In the case of 3-methylglutaconic aciduria type 5, NGS genetic testing can be used to identify mutations or variations in the DNAJC19 gene that may be responsible for the condition. NGS genetic testing can help in the diagnosis of 3-methylglutaconic aciduria type 5 by detecting specific genetic changes in the DNAJC19 gene. This information can be used to confirm the diagnosis, provide genetic counseling, and guide treatment decisions. It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the results. |
