ARSB Gene Mucopolysaccharidosis type 6 Genetic Test
Cost: AED 4400.0
Test Name: ARSB Gene Mucopolysaccharidosis type 6 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: AED 4400.0
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 ARSB Gene Mucopolysaccharidosis type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 6
Test Details: The ARSB gene is associated with the development of Mucopolysaccharidosis type 6 (MPS6), also known as Maroteaux-Lamy syndrome. MPS6 is a rare genetic disorder that affects the metabolism of complex sugar molecules called glycosaminoglycans (GAGs).
NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of MPS6, NGS can be used to identify mutations or variations in the ARSB gene that may be responsible for the development of the disorder. By sequencing the entire ARSB gene, NGS can detect various types of genetic alterations, such as single nucleotide variants (SNVs), small insertions or deletions (indels), and larger structural variations. This comprehensive analysis helps to identify specific mutations or variations that can lead to MPS6.
NGS genetic testing for ARSB gene mutations can be used for diagnostic purposes, allowing healthcare professionals to confirm the presence of MPS6 in individuals with suspected symptoms. It can also be used for carrier testing to identify individuals who may carry a single copy of the mutated gene but do not exhibit symptoms themselves. This information is crucial for family planning and genetic counseling.
Overall, NGS genetic testing for the ARSB gene in the context of MPS6 provides a powerful tool for accurate diagnosis, carrier testing, and genetic counseling for individuals and families affected by this rare genetic disorder.
| Test Name | ARSB Gene Mucopolysaccharidosis type 6 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 ARSB Gene Mucopolysaccharidosis type 6 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 6 |
| Test Details |
The ARSB gene is associated with the development of Mucopolysaccharidosis type 6 (MPS6), also known as Maroteaux-Lamy syndrome. MPS6 is a rare genetic disorder that affects the metabolism of complex sugar molecules called glycosaminoglycans (GAGs). NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of MPS6, NGS can be used to identify mutations or variations in the ARSB gene that may be responsible for the development of the disorder. By sequencing the entire ARSB gene, NGS can detect various types of genetic alterations, such as single nucleotide variants (SNVs), small insertions or deletions (indels), and larger structural variations. This comprehensive analysis helps to identify specific mutations or variations that can lead to MPS6. NGS genetic testing for ARSB gene mutations can be used for diagnostic purposes, allowing healthcare professionals to confirm the presence of MPS6 in individuals with suspected symptoms. It can also be used for carrier testing to identify individuals who may carry a single copy of the mutated gene but do not exhibit symptoms themselves. This information is crucial for family planning and genetic counseling. Overall, NGS genetic testing for the ARSB gene in the context of MPS6 provides a powerful tool for accurate diagnosis, carrier testing, and genetic counseling for individuals and families affected by this rare genetic disorder. |
