ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency Genetic Test
At DNA Labs UAE, we offer the ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency Genetic Test. This test helps analyze the ALDH6A1 gene for mutations or variations associated with methylmalonate semialdehyde dehydrogenase deficiency, a rare genetic disorder affecting the body’s ability to break down certain amino acids and organic acids.
Test Components and Price
Test Name: ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
Sample Condition and Report Delivery
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type and Method
Test Type: Metabolic Disorders
Method: NGS Technology
Referring Doctor and Test Department
Doctor: General Physician
Test Department: Genetics
Pre Test Information
Before undergoing the ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session is advised to draw a pedigree chart of family members affected with Methylmalonate semialdehyde dehydrogenase deficiency.
Test Details
The ALDH6A1 gene methylmalonate semialdehyde dehydrogenase deficiency NGS genetic test utilizes next-generation sequencing (NGS) technology to analyze the ALDH6A1 gene for mutations or variations associated with methylmalonate semialdehyde dehydrogenase deficiency. This rare genetic disorder impairs the body’s ability to break down certain amino acids and organic acids due to mutations in the ALDH6A1 gene, which codes for the methylmalonate semialdehyde dehydrogenase enzyme.
NGS genetic testing allows for the simultaneous analysis of multiple genes, including ALDH6A1, in a cost-effective and efficient manner. By sequencing the entire coding region of the ALDH6A1 gene, this test can identify any variations or mutations present. The results of this genetic test aid in the diagnosis of methylmalonate semialdehyde dehydrogenase deficiency and provide information about the specific genetic variant(s) involved.
These results are valuable for guiding treatment decisions, providing genetic counseling, and assessing the risk of passing the condition on to future generations. It is crucial to note that genetic testing should be performed and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can offer appropriate counseling and guidance based on the results.
| Test Name | ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency 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 ALDH6A1 Gene Methylmalonate semialdehyde dehydrogenase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonate semialdehyde dehydrogenase deficiency |
| Test Details |
ALDH6A1 gene methylmalonate semialdehyde dehydrogenase deficiency NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the ALDH6A1 gene for mutations or variations that may be associated with methylmalonate semialdehyde dehydrogenase deficiency. Methylmalonate semialdehyde dehydrogenase deficiency is a rare genetic disorder that affects the body’s ability to break down certain amino acids and organic acids. This deficiency is caused by mutations in the ALDH6A1 gene, which provides instructions for making an enzyme called methylmalonate semialdehyde dehydrogenase. NGS genetic testing allows for the simultaneous analysis of multiple genes, including the ALDH6A1 gene, in a cost-effective and efficient manner. By sequencing the entire coding region of the ALDH6A1 gene, this test can identify any variations or mutations that may be present. The results of this genetic test can help diagnose methylmalonate semialdehyde dehydrogenase deficiency and provide information about the specific genetic variant(s) involved. This information can be useful for guiding treatment decisions, providing genetic counseling, and assessing the risk of passing the condition on to future generations. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the results. |
