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PEX14 Gene Zellweger Syndrome Genetic Test Cost

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

-21%

The PEX14 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool designed to identify mutations in the PEX14 gene, which are linked to Zellweger Syndrome, a rare genetic disorder. This condition falls under the spectrum of peroxisome biogenesis disorders and is characterized by the impairment of multiple systems in the body, including the brain, liver, and kidneys. Early detection through genetic testing can provide crucial information for managing the syndrome, allowing for tailored treatments and interventions.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the PEX14 gene to uncover any genetic abnormalities that could indicate the presence of Zellweger Syndrome. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed using advanced genetic sequencing techniques to identify mutations.

The cost of the PEX14 Gene Zellweger Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate processes involved in genetic analysis and the specialized expertise required to interpret the results accurately. For families and individuals facing the possibility of Zellweger Syndrome, this test represents a critical step towards understanding the condition and planning for the necessary medical and supportive care.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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PEX14 Gene Zellweger Syndrome Genetic Test

Cost: AED 4400.0

Test Components:

  • Price: AED 4400.0
  • 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 PEX14 Gene Zellweger Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PEX14 Gene Zellweger Syndrome.

Test Details:

The PEX14 gene is associated with Zellweger Syndrome, a rare genetic disorder that affects multiple organs and systems in the body. Zellweger Syndrome is part of a group of disorders called peroxisome biogenesis disorders (PBDs), which are characterized by the impaired function of peroxisomes, cell organelles involved in various metabolic processes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technologies to rapidly sequence and analyze DNA samples.

NGS testing can be used to identify mutations or variations in genes associated with specific genetic disorders, including Zellweger Syndrome. Therefore, a PEX14 gene NGS genetic test would involve sequencing the PEX14 gene to identify any mutations or variations that may be causing or contributing to Zellweger Syndrome.

This information can be used for diagnostic purposes, genetic counseling, and potentially for guiding treatment decisions or management strategies for individuals with Zellweger Syndrome.

Test Name PEX14 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 PEX14 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX14 Gene Zellweger syndrome
Test Details

The PEX14 gene is associated with Zellweger syndrome, a rare genetic disorder that affects multiple organs and systems in the body. Zellweger syndrome is part of a group of disorders called peroxisome biogenesis disorders (PBDs), which are characterized by the impaired function of peroxisomes, which are cell organelles involved in various metabolic processes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technologies to rapidly sequence and analyze DNA samples. NGS testing can be used to identify mutations or variations in genes associated with specific genetic disorders, including Zellweger syndrome.

Therefore, a PEX14 gene NGS genetic test would involve sequencing the PEX14 gene to identify any mutations or variations that may be causing or contributing to Zellweger syndrome. This information can be used for diagnostic purposes, genetic counseling, and potentially for guiding treatment decisions or management strategies for individuals with Zellweger syndrome.

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