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PEX26 Gene Zellweger Syndrome Genetic Test Cost

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

-21%

The PEX26 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool used to detect mutations in the PEX26 gene, which is crucial for diagnosing Zellweger Syndrome, a rare, inherited disorder characterized by the absence or malfunction of peroxisomes in the cells of the body. This condition leads to a spectrum of medical issues, including impairments in the brain, liver, and kidneys, and affects physical and mental development.

The test is conducted by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab to identify any genetic alterations in the PEX26 gene.

The cost of the PEX26 Gene Zellweger Syndrome Genetic Test is 4400 AED. This investment is crucial for families seeking answers to health questions related to Zellweger Syndrome, as early detection and understanding of the specific genetic mutation can guide treatment options, manage symptoms, and improve the quality of life for affected individuals.

Description

PEX26 Gene Zellweger Syndrome Genetic Test

Test Name: PEX26 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 PEX26 Gene Zellweger Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX26 Gene Zellweger Syndrome.

Test Details:

The PEX26 Gene Zellweger Syndrome NGS Genetic Test is a type of genetic test that focuses on analyzing the PEX26 gene for mutations associated with Zellweger syndrome. Zellweger syndrome is a rare genetic disorder that affects the development and function of many organs in the body.

NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes, making it an efficient and cost-effective method for genetic testing. In the case of the PEX26 Gene Zellweger Syndrome NGS Genetic Test, it involves sequencing the entire PEX26 gene to identify any mutations or variations that may be causing or contributing to the development of Zellweger syndrome.

This genetic test can help in diagnosing Zellweger syndrome, providing information about the specific genetic mutation causing the disorder, and assisting in genetic counseling and family planning. It can also be used for carrier testing to identify individuals who carry a mutation in the PEX26 gene but do not have symptoms of Zellweger syndrome themselves.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling to ensure accurate and appropriate interpretation of the results.

Test Name	PEX26 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 PEX26 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX26 Gene Zellweger syndrome
Test Details	PEX26 gene Zellweger syndrome NGS genetic test is a type of genetic test that focuses on analyzing the PEX26 gene for mutations associated with Zellweger syndrome. Zellweger syndrome is a rare genetic disorder that affects the development and function of many organs in the body. NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes, making it an efficient and cost-effective method for genetic testing. In the case of PEX26 gene Zellweger syndrome NGS genetic test, it involves sequencing the entire PEX26 gene to identify any mutations or variations that may be causing or contributing to the development of Zellweger syndrome. This genetic test can help in diagnosing Zellweger syndrome, providing information about the specific genetic mutation causing the disorder, and assisting in genetic counseling and family planning. It can also be used for carrier testing to identify individuals who carry a mutation in the PEX26 gene but do not have symptoms of Zellweger syndrome themselves. It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling to ensure accurate and appropriate interpretation of the results.