PEX1 Gene Zellweger Syndrome Genetic Test
Cost: AED 4400.0
Test Name: PEX1 Gene Zellweger Syndrome Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for PEX1 Gene Zellweger Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX1 Gene Zellweger Syndrome.
The PEX1 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects multiple systems in the body, including the brain, liver, and kidneys. Zellweger syndrome is caused by mutations in genes involved in peroxisome biogenesis, and the PEX1 gene is one of the genes commonly affected.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Zellweger syndrome, NGS genetic testing can be used to identify mutations in the PEX1 gene and other related genes that may be responsible for the disorder.
NGS genetic testing can provide a comprehensive analysis of multiple genes at once, allowing for a more efficient and accurate diagnosis of Zellweger syndrome. It can also help in identifying carriers of the gene mutations and provide information for genetic counseling and family planning.
It is important to note that genetic testing for Zellweger syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.
| Test Name | PEX1 Gene Zellweger syndrome Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PEX1 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX1 Gene Zellweger syndrome |
| Test Details |
The PEX1 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects multiple systems in the body, including the brain, liver, and kidneys. Zellweger syndrome is caused by mutations in genes involved in peroxisome biogenesis, and the PEX1 gene is one of the genes commonly affected. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Zellweger syndrome, NGS genetic testing can be used to identify mutations in the PEX1 gene and other related genes that may be responsible for the disorder. NGS genetic testing can provide a comprehensive analysis of multiple genes at once, allowing for a more efficient and accurate diagnosis of Zellweger syndrome. It can also help in identifying carriers of the gene mutations and provide information for genetic counseling and family planning. It is important to note that genetic testing for Zellweger syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support. |
