PEX19 Gene Zellweger Syndrome Genetic Test
Test Name: PEX19 Gene Zellweger Syndrome Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for PEX19 Gene Zellweger Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX19 Gene Zellweger Syndrome.
Test Details
The PEX19 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects the development and function of the peroxisomes, which are cellular structures involved in various metabolic processes. Mutations in the PEX19 gene can lead to impaired peroxisome biogenesis, resulting in the characteristic symptoms of Zellweger syndrome.
NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of genetic testing for Zellweger syndrome, NGS can be used to analyze the PEX19 gene for any disease-causing mutations. This can help in confirming a diagnosis of Zellweger syndrome and providing information about the specific genetic variant involved.
NGS genetic testing for Zellweger syndrome can be performed on a blood or tissue sample. The DNA is extracted from the sample and then sequenced using NGS technology. The resulting sequence data is then analyzed to identify any mutations or variants in the PEX19 gene that may be associated with Zellweger syndrome.
Genetic testing for Zellweger syndrome can be helpful for individuals with suspected symptoms or a family history of the condition. It can provide a definitive diagnosis, inform genetic counseling, and help with family planning decisions. However, it is important to note that genetic testing may not be able to identify all possible mutations or variants in the PEX19 gene, and a negative result does not completely rule out the possibility of Zellweger syndrome. Therefore, clinical evaluation and other diagnostic tests may still be necessary in some cases.
| Test Name | PEX19 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 PEX19 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX19 Gene Zellweger syndrome |
| Test Details |
The PEX19 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects the development and function of the peroxisomes, which are cellular structures involved in various metabolic processes. Mutations in the PEX19 gene can lead to impaired peroxisome biogenesis, resulting in the characteristic symptoms of Zellweger syndrome. NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of genetic testing for Zellweger syndrome, NGS can be used to analyze the PEX19 gene for any disease-causing mutations. This can help in confirming a diagnosis of Zellweger syndrome and providing information about the specific genetic variant involved. NGS genetic testing for Zellweger syndrome can be performed on a blood or tissue sample. The DNA is extracted from the sample and then sequenced using NGS technology. The resulting sequence data is then analyzed to identify any mutations or variants in the PEX19 gene that may be associated with Zellweger syndrome. Genetic testing for Zellweger syndrome can be helpful for individuals with suspected symptoms or a family history of the condition. It can provide a definitive diagnosis, inform genetic counseling, and help with family planning decisions. However, it is important to note that genetic testing may not be able to identify all possible mutations or variants in the PEX19 gene, and a negative result does not completely rule out the possibility of Zellweger syndrome. Therefore, clinical evaluation and other diagnostic tests may still be necessary in some cases. |
