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PEX16 Gene Zellweger Syndrome Genetic Test Cost

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

-21%

The PEX16 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic assessment designed to detect mutations in the PEX16 gene, which are associated with Zellweger Syndrome, a rare genetic disorder. This condition belongs to a group of diseases known as peroxisome biogenesis disorders, characterized by the body’s inability to properly form peroxisomes, leading to severe metabolic complications. The PEX16 gene plays a crucial role in the formation of peroxisomes, and mutations in this gene can disrupt cellular processes, resulting in the symptoms observed in Zellweger Syndrome, which include developmental delays, neurological issues, and abnormalities in liver and kidney function.

Conducted at DNA Labs UAE, a leading genetic testing facility known for its advanced diagnostic technologies and expertise in genetic analysis, this test offers families and individuals critical information regarding the genetic underpinnings of Zellweger Syndrome. The test is priced at 4400 AED, reflecting the sophisticated nature of the genetic analysis and the specialized expertise required to interpret the results. Through a simple blood sample, the test aims to provide conclusive evidence of the presence or absence of mutations in the PEX16 gene, offering invaluable insights for affected families. This information can guide treatment decisions, inform family planning, and connect families with appropriate support and resources for managing the condition.

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  • This test is not intended for medical diagnosis or treatment
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PEX16 Gene Zellweger Syndrome Genetic Test

At DNA Labs UAE, we offer the PEX16 Gene Zellweger Syndrome Genetic Test to help diagnose and manage this rare genetic disorder. Zellweger syndrome affects the development and function of peroxisomes in cells, which play a crucial role in metabolic processes.

Test Components and Price

The PEX16 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

After conducting the test, we deliver the report within 3 to 4 weeks.

Method

We utilize Next-Generation Sequencing (NGS) technology to analyze the individual’s DNA for variations or mutations within the PEX16 gene.

Test Type and Doctor

The PEX16 Gene Zellweger Syndrome Genetic Test falls under the category of Neurological Disorders. Our team of experienced neurologists handles this test in our Genetics department.

Pre Test Information

Before conducting the PEX16 Gene Zellweger Syndrome Genetic Test, we require the patient’s clinical history. Additionally, a genetic counseling session is conducted to create a pedigree chart of family members affected by this genetic disorder.

Test Details

Zellweger syndrome is a rare genetic disorder caused by mutations in the PEX16 gene. This gene is responsible for the proper functioning of peroxisomes, which are involved in metabolic processes such as fatty acid breakdown and lipid production.

Our NGS genetic test analyzes the individual’s DNA to identify any variations or mutations within the PEX16 gene. By detecting mutations that disrupt the normal function of this gene, we can provide an accurate diagnosis of Zellweger syndrome.

NGS technology allows for the simultaneous sequencing of multiple genes or even the entire genome, making it a powerful tool for genetic testing. With the identification of PEX16 gene mutations, healthcare professionals can offer appropriate medical management and genetic counseling to affected individuals and their families.

Test Name PEX16 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 PEX16 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX16 Gene Zellweger syndrome
Test Details

The PEX16 gene is associated with Zellweger syndrome, a rare genetic disorder that affects the development and function of the peroxisomes in cells. Peroxisomes are responsible for various metabolic processes, including the breakdown of fatty acids and the production of certain lipids.

A Next-Generation Sequencing (NGS) genetic test for the PEX16 gene involves analyzing the individual’s DNA to identify any variations or mutations within the gene. This test can help diagnose Zellweger syndrome by detecting mutations that disrupt the normal function of the PEX16 gene.

NGS technology allows for the simultaneous sequencing of multiple genes or even the entire genome, making it a powerful tool for genetic testing. By identifying mutations in the PEX16 gene, healthcare professionals can provide an accurate diagnosis of Zellweger syndrome and offer appropriate medical management and genetic counseling for affected individuals and their families.

SKU: TEST-2119 Category:

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