GNS Gene Mucopolysaccharidosis type 3D Genetic Test
Test Name: GNS Gene Mucopolysaccharidosis type 3D Genetic Test
Components: DNA Labs UAE
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 GNS Gene Mucopolysaccharidosis type 3D NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 3D.
Test Details:
The GNS gene is associated with a genetic disorder called Mucopolysaccharidosis type 3D (MPS 3D), also known as Sanfilippo syndrome type D. MPS 3D is a rare inherited metabolic disorder characterized by the accumulation of complex sugar molecules called glycosaminoglycans (GAGs) in various tissues and organs of the body.
NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of genetic testing for MPS 3D, NGS can be used to identify mutations or variants in the GNS gene that may be responsible for the disorder.
The NGS genetic test for MPS 3D involves obtaining a DNA sample, usually through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variants in the GNS gene. These genetic changes can help confirm a diagnosis of MPS 3D and provide information about the specific genetic variant causing the disorder.
Genetic testing for MPS 3D can be helpful in confirming a diagnosis, guiding treatment decisions, and providing information about the risk of passing the disorder on to future generations. It can also be useful for carrier testing in individuals with a family history of MPS 3D.
It is important to note that genetic testing for MPS 3D should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.
Test Name | GNS Gene Mucopolysaccharidosis type 3D 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 GNS Gene Mucopolysaccharidosis type 3D NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 3D |
Test Details |
The GNS gene is associated with a genetic disorder called Mucopolysaccharidosis type 3D (MPS 3D), also known as Sanfilippo syndrome type D. MPS 3D is a rare inherited metabolic disorder characterized by the accumulation of complex sugar molecules called glycosaminoglycans (GAGs) in various tissues and organs of the body. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of genetic testing for MPS 3D, NGS can be used to identify mutations or variants in the GNS gene that may be responsible for the disorder. The NGS genetic test for MPS 3D involves obtaining a DNA sample, usually through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variants in the GNS gene. These genetic changes can help confirm a diagnosis of MPS 3D and provide information about the specific genetic variant causing the disorder. Genetic testing for MPS 3D can be helpful in confirming a diagnosis, guiding treatment decisions, and providing information about the risk of passing the disorder on to future generations. It can also be useful for carrier testing in individuals with a family history of MPS 3D. It is important to note that genetic testing for MPS 3D should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support. |