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PEX13 Gene Zellweger Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PEX13 gene plays a crucial role in the development of Zellweger syndrome, a rare genetic disorder that affects multiple systems in the body. Zellweger syndrome is part of a group of diseases known as peroxisome biogenesis disorders (PBDs), which are characterized by the cells’ inability to properly assemble peroxisomes. These peroxisomes are essential for various cellular processes, including the breakdown of fatty acids and the detoxification of hydrogen peroxide. Mutations in the PEX13 gene disrupt these vital cellular functions, leading to the severe symptoms observed in Zellweger syndrome, which can include developmental delays, neurological issues, and abnormalities in liver and kidney function.

To diagnose Zellweger syndrome, genetic testing of the PEX13 gene can be conducted. DNA Labs UAE offers a comprehensive genetic test for the PEX13 gene to confirm the diagnosis of Zellweger syndrome. This test is crucial for families seeking answers about this genetic condition, as it can provide definitive evidence of the disorder and help guide treatment and management decisions.

The cost of the PEX13 gene Zellweger syndrome genetic test at DNA Labs UAE is 4400 AED. While the price may seem significant, the test offers invaluable information for affected families, enabling them to understand the genetic basis of the condition and consider their options for care and support. It is important for prospective patients or their families to consult with a genetic counselor or healthcare provider to discuss the benefits and implications of genetic testing for Zellweger syndrome.

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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.