PEX13 Gene Zellweger syndrome 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
Neurological Disorders
Doctor
Neurologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for PEX13 Gene Zellweger syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX13 Gene Zellweger syndrome.
Test Details
The PEX13 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects the development and function of the peroxisomes. Peroxisomes are cellular structures that play a crucial role in various metabolic processes. NGS (Next-Generation Sequencing) is a type of genetic test that can be used to analyze the DNA sequence of the PEX13 gene. This test can identify any mutations or changes in the gene that may be responsible for causing Zellweger syndrome. By analyzing the PEX13 gene using NGS, healthcare professionals can determine if there are any genetic abnormalities that could lead to the development of Zellweger syndrome. This information can be used for diagnostic purposes, genetic counseling, and to guide the management and treatment of individuals with this condition.
Test Name | PEX13 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 PEX13 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX13 Gene Zellweger syndrome |
Test Details |
The PEX13 gene is associated with Zellweger syndrome, which is a rare genetic disorder that affects the development and function of the peroxisomes. Peroxisomes are cellular structures that play a crucial role in various metabolic processes. NGS (Next-Generation Sequencing) is a type of genetic test that can be used to analyze the DNA sequence of the PEX13 gene. This test can identify any mutations or changes in the gene that may be responsible for causing Zellweger syndrome. By analyzing the PEX13 gene using NGS, healthcare professionals can determine if there are any genetic abnormalities that could lead to the development of Zellweger syndrome. This information can be used for diagnostic purposes, genetic counseling, and to guide the management and treatment of individuals with this condition. |