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DRD2 Gene DYT11 DRD2 Related Genetic Test

4,400 د.إ

-21%

The DRD2 gene, associated with the dopamine D2 receptor, plays a critical role in the brain’s dopaminergic system, influencing various neurological functions. Mutations or variations in this gene have been linked to several disorders, including DYT11, a condition characterized by myoclonus-dystonia. This genetic disorder involves involuntary muscle jerking (myoclonus) and dystonia, leading to repetitive muscle contractions resulting in twisting and abnormal postures.

The DRD2 Related Genetic Test is a specific diagnostic tool aimed at identifying mutations in the DRD2 gene that are connected to DYT11. Conducted at DNA Labs UAE, this test is pivotal for individuals displaying symptoms of myoclonus-dystonia or those with a family history of the condition, providing crucial information for diagnosis, treatment planning, and genetic counseling.

The test is priced at 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it offers into the patient’s genetic makeup regarding the DRD2 gene. By opting for this test, patients and healthcare providers can make informed decisions regarding the management of conditions related to DRD2 gene mutations, potentially improving quality of life and outcomes for those affected.

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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DRD2 Gene DYT11 DRD2 related Genetic Test

At DNA Labs UAE, we offer the DRD2 Gene DYT11 DRD2 related Genetic Test for individuals who suspect they may have DYT11, a rare form of inherited dystonia. This genetic test can help diagnose the condition and develop personalized treatment plans.

Test Details

The DRD2 gene is associated with DYT11, a rare form of inherited dystonia that affects the muscles of the body, causing them to contract and spasm uncontrollably. A NGS (next-generation sequencing) genetic test can be used to analyze the DRD2 gene and identify any mutations or variants that may be contributing to the development of DYT11. This test involves sequencing the entire gene to identify any changes in the DNA sequence that may be affecting the function of the DRD2 protein. This information can be used to diagnose DYT11 and develop personalized treatment plans for affected individuals.

Test Components and Price

  • Test Name: DRD2 Gene DYT11 DRD2 related Genetic Test
  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card for the DRD2 Gene DYT11 DRD2 related Genetic Test.

Report Delivery

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

Method

The DRD2 Gene DYT11 DRD2 related Genetic Test utilizes NGS (next-generation sequencing) technology.

Test Type

The DRD2 Gene DYT11 DRD2 related Genetic Test is specifically designed for diagnosing neurological disorders.

Doctor and Test Department

The test is performed by a neurologist in our Genetics Test Department.

Pre Test Information

Prior to undergoing the DRD2 Gene DYT11 DRD2 related Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with DRD2 Gene DYT11, DRD2 related.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name DRD2 Gene DYT11 DRD2 related 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 DRD2 Gene DYT11, DRD2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DRD2 Gene DYT11, DRD2 related
Test Details

The DRD2 gene is associated with DYT11, a rare form of inherited dystonia that affects the muscles of the body, causing them to contract and spasm uncontrollably. A NGS (next-generation sequencing) genetic test can be used to analyze the DRD2 gene and identify any mutations or variants that may be contributing to the development of DYT11. This test involves sequencing the entire gene to identify any changes in the DNA sequence that may be affecting the function of the DRD2 protein. This information can be used to diagnose DYT11 and develop personalized treatment plans for affected individuals.