BTD Gene Biotinidase deficiency Genetic Test
Components: BTD gene biotinidase deficiency NGS genetic test
Price: 3200.0 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 BTD Gene Biotinidase deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Biotinidase deficiency
Test Details
BTD gene biotinidase deficiency NGS genetic test is a type of genetic test that analyzes the BTD gene for mutations or variations that may cause biotinidase deficiency. Biotinidase deficiency is a rare inherited metabolic disorder that affects the body’s ability to process biotin, a vitamin essential for the metabolism of fats, proteins, and carbohydrates.
The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the BTD gene, in a more efficient and cost-effective manner compared to traditional sequencing methods.
The test involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BTD gene that may be associated with biotinidase deficiency.
The results of the test can provide valuable information about an individual’s genetic predisposition to biotinidase deficiency. This information can be used for diagnosis, genetic counseling, and potentially for guiding treatment options.
It is important to note that the BTD gene biotinidase deficiency NGS genetic test is a medical test that should be ordered and interpreted by healthcare professionals, such as geneticists or genetic counselors, who have expertise in genetic testing and counseling.
| Test Name | BTD Gene Biotinidase deficiency Genetic Test |
|---|---|
| Components | |
| Price | 3200.0 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 BTD Gene Biotinidase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Biotinidase deficiency |
| Test Details |
BTD gene biotinidase deficiency NGS genetic test is a type of genetic test that analyzes the BTD gene for mutations or variations that may cause biotinidase deficiency. Biotinidase deficiency is a rare inherited metabolic disorder that affects the body’s ability to process biotin, a vitamin essential for the metabolism of fats, proteins, and carbohydrates. The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the BTD gene, in a more efficient and cost-effective manner compared to traditional sequencing methods. The test involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BTD gene that may be associated with biotinidase deficiency. The results of the test can provide valuable information about an individual’s genetic predisposition to biotinidase deficiency. This information can be used for diagnosis, genetic counseling, and potentially for guiding treatment options. It is important to note that the BTD gene biotinidase deficiency NGS genetic test is a medical test that should be ordered and interpreted by healthcare professionals, such as geneticists or genetic counselors, who have expertise in genetic testing and counseling. |
