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LRRK2 Gene PARK8 Parkinson Genetic Test Cost

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

-21%

The LRRK2 Gene PARK8 Parkinson Genetic Test is a specialized diagnostic tool designed to identify mutations in the LRRK2 gene, which is known to be a significant genetic factor in the development of Parkinson’s disease. This gene, also referred to as PARK8, plays a crucial role in the functioning of neurons in the brain, and mutations within this gene can lead to the onset of Parkinson’s disease, characterized by symptoms such as tremors, stiffness, and difficulty with balance and coordination.

Offered at DNA Labs UAE, this test is aimed at individuals who have a family history of Parkinson’s disease or are experiencing symptoms associated with the condition, providing them with valuable information regarding their genetic predisposition. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any alterations in the LRRK2 gene.

The cost of the LRRK2 Gene PARK8 Parkinson Genetic Test at DNA Labs UAE is 4400 AED. This investment can be invaluable for individuals seeking early detection and a deeper understanding of their risk factors for developing Parkinson’s disease. Early diagnosis can significantly impact management and treatment options, potentially improving quality of life.

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  • This test is not intended for medical diagnosis or treatment
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LRRK2 Gene PARK8 Parkinson Genetic Test

At DNA Labs UAE, we offer the LRRK2 Gene PARK8 Parkinson Genetic Test to assess the risk of developing Parkinson’s disease. This test is designed to analyze the LRRK2 gene, specifically in the PARK8 locus, which has been identified as a cause of familial Parkinson’s disease.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

After the test is conducted, the report will be delivered within 3 to 4 weeks.

Method

The LRRK2 Gene PARK8 Parkinson Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This method allows for the simultaneous analysis of multiple genes for mutations or variations.

Test Type

The LRRK2 Gene PARK8 Parkinson Genetic Test falls under the category of Neurological Disorders.

Doctor

The test is conducted under the supervision of a Neurologist.

Test Department

The LRRK2 Gene PARK8 Parkinson Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the LRRK2 Gene PARK8 Parkinson NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by LRRK2 Gene PARK8 Parkinson.

Test Details

The LRRK2 gene is associated with an increased risk of developing Parkinson’s disease. Mutations in this gene, specifically in the PARK8 locus, have been identified as a cause of familial Parkinson’s disease.

NGS genetic testing is a method used to analyze multiple genes simultaneously for mutations or variations. In the context of Parkinson’s disease, NGS genetic testing can be used to identify mutations in the LRRK2 gene that may contribute to the development of the disease.

By analyzing the LRRK2 gene through NGS genetic testing, healthcare professionals can provide individuals with information about their genetic risk for Parkinson’s disease. This information can be useful for early detection, prevention, and personalized treatment plans.

It is important to note that not all individuals with LRRK2 mutations will develop Parkinson’s disease, as other factors, both genetic and environmental, can influence the disease’s onset and progression.

Test Name LRRK2 Gene PARK8 Parkinson 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 LRRK2 Gene PARK8 Parkinson NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LRRK2 Gene PARK8 Parkinson
Test Details

The LRRK2 gene is associated with an increased risk of developing Parkinson’s disease. Mutations in this gene, specifically in the PARK8 locus, have been identified as a cause of familial Parkinson’s disease.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for mutations or variations. In the context of Parkinson’s disease, NGS genetic testing can be used to identify mutations in the LRRK2 gene that may contribute to the development of the disease.

By analyzing the LRRK2 gene through NGS genetic testing, healthcare professionals can provide individuals with information about their genetic risk for Parkinson’s disease. This information can be useful for early detection, prevention, and personalized treatment plans. It is important to note that not all individuals with LRRK2 mutations will develop Parkinson’s disease, as other factors, both genetic and environmental, can influence the disease’s onset and progression.