PEX2 Gene Zellweger Syndrome Genetic Test
At DNA Labs UAE, we offer the PEX2 Gene Zellweger Syndrome Genetic Test to help diagnose and provide valuable information for genetic counseling, prognosis, and potential treatment options for Zellweger syndrome. Zellweger syndrome is a rare genetic disorder that affects the development and function of many organs in the body.
Test Components and Price
The PEX2 Gene Zellweger Syndrome Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA Card.
Report Delivery and Test Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, allowing for the sequencing of multiple genes simultaneously.
Test Type and Doctor
The PEX2 Gene Zellweger Syndrome Genetic Test falls under the category of Neurological Disorders. The test is conducted by a Neurologist in our Genetics department.
Pre Test Information
Before undergoing the PEX2 Gene Zellweger Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with PEX2 Gene Zellweger syndrome.
About Zellweger Syndrome and NGS Genetic Testing
Zellweger syndrome is part of a group of disorders called peroxisome biogenesis disorders (PBDs). The PEX2 gene is associated with Zellweger syndrome. NGS genetic testing allows for the analysis of the PEX2 gene to identify any mutations or variations that may be associated with the condition. By identifying these mutations, the test helps diagnose Zellweger syndrome and provides valuable information for genetic counseling, prognosis, and potential treatment options.
| Test Name | PEX2 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 PEX2 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX2 Gene Zellweger syndrome |
| Test Details |
The PEX2 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects the development and function of many organs in the body. Zellweger syndrome is part of a group of disorders called peroxisome biogenesis disorders (PBDs). NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the sequencing of multiple genes simultaneously. In the context of Zellweger syndrome, NGS genetic testing can be used to analyze the PEX2 gene for any mutations or variations that may be associated with the condition. By identifying mutations in the PEX2 gene, NGS genetic testing can help diagnose Zellweger syndrome and provide valuable information for genetic counseling, prognosis, and potential treatment options. |
