PEX6 Gene Zellweger Syndrome Genetic Test sale cost 4400 AED
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PEX6 Gene Zellweger Syndrome Genetic Test Cost

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

-21%

The PEX6 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PEX6 gene, which are linked to Zellweger Syndrome. Zellweger Syndrome is a rare, inherited disorder characterized by the reduction or absence of peroxisomes in the cells of the body, leading to a spectrum of medical issues including abnormalities in the brain, liver, and kidneys, as well as developmental delays. The test is crucial for early diagnosis and management of the condition, providing essential genetic information that can guide treatment plans and inform family planning decisions. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the presence of PEX6 gene mutations. Conducted at DNA Labs UAE, this test is an important tool for families and individuals at risk of Zellweger Syndrome, offering hope for better management of the condition through early detection and intervention.

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PEX6 Gene Zellweger Syndrome Genetic Test

Components

  • Test Name: PEX6 Gene Zellweger Syndrome Genetic Test
  • 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 PEX6 Gene Zellweger Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX6 Gene Zellweger Syndrome.

Test Details

The PEX6 gene is associated with Zellweger syndrome, a rare genetic disorder that affects the development and function of the peroxisomes, which are responsible for various metabolic processes in the body. Zellweger syndrome is characterized by severe neurological abnormalities, liver dysfunction, and other organ malformations.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any mutations or variants that may be present. In the case of Zellweger syndrome, NGS genetic testing can be used to detect mutations or variants in the PEX6 gene that may be causing the disorder.

By identifying the specific genetic mutation or variant, NGS genetic testing can help confirm a diagnosis of Zellweger syndrome and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of Zellweger syndrome or for prenatal testing in families at risk of having a child with the disorder.

Test Name PEX6 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 PEX6 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX6 Gene Zellweger syndrome
Test Details

The PEX6 gene is associated with Zellweger syndrome, a rare genetic disorder that affects the development and function of the peroxisomes, which are responsible for various metabolic processes in the body. Zellweger syndrome is characterized by severe neurological abnormalities, liver dysfunction, and other organ malformations.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify any mutations or variants that may be present. In the case of Zellweger syndrome, NGS genetic testing can be used to detect mutations or variants in the PEX6 gene that may be causing the disorder.

By identifying the specific genetic mutation or variant, NGS genetic testing can help confirm a diagnosis of Zellweger syndrome and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of Zellweger syndrome or for prenatal testing in families at risk of having a child with the disorder.

SKU: TEST-2123 Category:

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