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RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test Cost

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

-21%

The RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the RARS2 gene, which are linked to Pontocerebellar Hypoplasia Type 6 (PCH6). This condition is a rare genetic disorder characterized by the underdevelopment of the cerebellum and pons, two critical regions of the brain, leading to severe neurological impairments. Symptoms can include delayed development, motor skills difficulties, and in some cases, seizures.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test aims to provide conclusive genetic evidence for the diagnosis of PCH6. This is crucial for the management and treatment of the condition, allowing for tailored care plans and informed genetic counseling for affected families. The test involves collecting a DNA sample, typically through a blood draw, and then examining the RARS2 gene for specific mutations known to cause the disorder.

The cost of the RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the genetic variations associated with the condition, offering families critical insights into their genetic health and the potential risks for future offspring.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test

At DNA Labs UAE, we offer the RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test for individuals suspected of having this rare genetic disorder. This test can provide valuable insights into the underlying genetic cause of the disorder and assist in diagnosis, genetic counseling, and family planning.

Test Components

The RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test includes:

  • NGS Technology
  • Neurological Disorders Test Type
  • Genetics Test Department

Price

The cost of the RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test is AED 4400.0.

Sample Condition

We accept the following sample conditions for this test:

  • Blood
  • Extracted DNA
  • One drop of blood on FTA Card

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method

The RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test utilizes NGS (Next-Generation Sequencing) technology for analysis.

Doctor

This test is recommended to be conducted under the supervision of a Neurologist.

Test Department

The RARS2 Gene Pontocerebellar Hypoplasia Type 6 Genetic Test falls under the Genetics Test Department.

Pre Test Information

Prior to undergoing the RARS2 Gene Pontocerebellar Hypoplasia Type 6 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with RARS2 Gene Pontocerebellar Hypoplasia Type 6.

Test Details

The RARS2 gene is associated with a rare genetic disorder known as pontocerebellar hypoplasia type 6 (PCH6). This disorder is characterized by underdevelopment (hypoplasia) of the pons and cerebellum, resulting in neurological abnormalities and developmental delays.

NGS genetic testing allows for the simultaneous analysis of multiple genes. In the context of PCH6, NGS genetic testing can identify mutations or variations in the RARS2 gene that may be responsible for the disorder. By analyzing the DNA sequence of the RARS2 gene, NGS genetic testing can detect any changes in the gene associated with PCH6. This aids in confirming a diagnosis of PCH6, providing information about the specific genetic mutation involved, and assisting in genetic counseling and family planning.

It is crucial to note that genetic testing should be conducted and interpreted by qualified healthcare professionals or genetic counselors who can provide appropriate guidance and support.

Test Name RARS2 Gene Pontocerebellar hypoplasia type 6 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 RARS2 Gene Pontocerebellar hypoplasia type 6 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RARS2 Gene Pontocerebellar hypoplasia type 6
Test Details

The RARS2 gene is associated with a rare genetic disorder called pontocerebellar hypoplasia type 6 (PCH6). PCH6 is characterized by underdevelopment (hypoplasia) of the pons and cerebellum, leading to neurological abnormalities and developmental delays.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the context of PCH6, NGS genetic testing can be used to identify mutations or variations in the RARS2 gene that may be causing the disorder.

By analyzing the DNA sequence of the RARS2 gene, NGS genetic testing can detect any changes in the gene that may be associated with PCH6. This can help in confirming a diagnosis of PCH6, providing information about the specific genetic mutation involved, and assisting in genetic counseling and family planning.

It’s important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support.

SKU: TEST-1930 Category:

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