NADK2 Gene 24-dienoyl-CoA reductase deficiency Genetic Test
Test Name: NADK2 Gene 24-dienoyl-CoA reductase deficiency Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 NADK2 Gene 2,4-dienoyl-CoA reductase deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with 2,4-dienoyl-CoA reductase deficiency.
Test Details
The NADK2 gene is responsible for encoding the enzyme 2,4-dienoyl-CoA reductase, which plays a role in fatty acid metabolism. Deficiency in this enzyme can lead to a condition known as NADK2 gene 2,4-dienoyl-CoA reductase deficiency.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze a person’s DNA to identify genetic variations or mutations that may be associated with certain disorders or conditions. In the case of NADK2 gene 2,4-dienoyl-CoA reductase deficiency, NGS genetic testing can be used to identify any mutations or variations in the NADK2 gene that may be causing the deficiency.
This type of genetic testing involves sequencing the entire or specific regions of the NADK2 gene to identify any genetic changes that may be present. The results of the NGS genetic test can help in confirming a diagnosis of NADK2 gene 2,4-dienoyl-CoA reductase deficiency and can also provide information about the specific genetic variations or mutations present, which can be useful for genetic counseling and treatment planning.
It is important to note that NGS genetic testing may not be available in all healthcare settings and may require a referral to a specialized genetics laboratory or clinic. Additionally, the interpretation of the test results should be done by a qualified healthcare professional with expertise in genetics.
| Test Name | NADK2 Gene 24-dienoyl-CoA reductase 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 NADK2 Gene 2,4-dienoyl-CoA reductase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 2,4-dienoyl-CoA reductase deficiency |
| Test Details |
The NADK2 gene is responsible for encoding the enzyme 2,4-dienoyl-CoA reductase, which plays a role in fatty acid metabolism. Deficiency in this enzyme can lead to a condition known as NADK2 gene 2,4-dienoyl-CoA reductase deficiency. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze a person’s DNA to identify genetic variations or mutations that may be associated with certain disorders or conditions. In the case of NADK2 gene 2,4-dienoyl-CoA reductase deficiency, NGS genetic testing can be used to identify any mutations or variations in the NADK2 gene that may be causing the deficiency. This type of genetic testing involves sequencing the entire or specific regions of the NADK2 gene to identify any genetic changes that may be present. The results of the NGS genetic test can help in confirming a diagnosis of NADK2 gene 2,4-dienoyl-CoA reductase deficiency and can also provide information about the specific genetic variations or mutations present, which can be useful for genetic counseling and treatment planning. It is important to note that NGS genetic testing may not be available in all healthcare settings and may require a referral to a specialized genetics laboratory or clinic. Additionally, the interpretation of the test results should be done by a qualified healthcare professional with expertise in genetics. |
