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PEX10 Gene Zellweger Syndrome Genetic Test Cost

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

-21%

The PEX10 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool used to identify mutations in the PEX10 gene, which are linked to Zellweger Syndrome – a rare, inherited disorder characterized by the disruption of normal cellular functions. This condition falls under a group of diseases known as peroxisome biogenesis disorders, which affect multiple systems of the body and present severe symptoms right from infancy.

The test, which is available at DNA Labs UAE, is crucial for early detection and management of the syndrome. It involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific genetic anomalies associated with the disorder. The result aids in confirming the diagnosis, which can significantly impact treatment plans and patient care.

The cost of the PEX10 Gene Zellweger Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment is vital for families with a history of the disorder or those who have children presenting symptoms related to Zellweger Syndrome. Early and accurate diagnosis through this genetic testing can lead to better management of the condition and improve the quality of life for affected individuals.

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PEX10 Gene Zellweger Syndrome Genetic Test

At DNA Labs UAE, we offer the PEX10 Gene Zellweger Syndrome Genetic Test at a cost of 4400.0 AED. This test is used to diagnose Zellweger syndrome, a rare genetic disorder that affects multiple organs.

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

Before undergoing the PEX10 Gene Zellweger Syndrome Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by the syndrome.

Test Details

The PEX10 gene is associated with Zellweger syndrome, a rare genetic disorder that affects the brain, liver, and kidneys. This syndrome is characterized by the absence or malfunction of peroxisomes, which play a crucial role in metabolic processes within cells.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the case of Zellweger syndrome, NGS testing can identify mutations or variations in the PEX10 gene that may be responsible for the disorder. It provides a comprehensive analysis of the entire coding region of the gene, detecting various types of genetic alterations.

By identifying specific genetic variants in the PEX10 gene, NGS testing confirms a diagnosis of Zellweger syndrome and offers valuable information for genetic counseling and family planning. It can also be used for carrier screening in individuals with a family history of the syndrome or for prenatal testing in at-risk pregnancies.

Test Name PEX10 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 PEX10 Gene Zellweger syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX10 Gene Zellweger syndrome
Test Details

The PEX10 gene is associated with Zellweger syndrome, a rare genetic disorder that affects multiple organs, including the brain, liver, and kidneys. Zellweger syndrome is characterized by the absence or malfunction of peroxisomes, which are responsible for various metabolic processes within cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the context of Zellweger syndrome, NGS genetic testing can be used to identify mutations or variations in the PEX10 gene that may be responsible for the disorder.

NGS testing can provide a comprehensive analysis of the entire coding region of the PEX10 gene, allowing for the detection of various types of genetic alterations, including small nucleotide changes (point mutations), insertions, deletions, and larger structural variants.

By identifying specific genetic variants in the PEX10 gene, NGS testing can help confirm a diagnosis of Zellweger syndrome and provide valuable information for genetic counseling and family planning. Additionally, NGS testing may also be used for carrier screening in individuals with a family history of Zellweger syndrome or for prenatal testing in at-risk pregnancies.

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