Sale!

PRKRA Gene DYT16 Genetic Test

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

-21%

The PRKRA Gene DYT16 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the PRKRA gene, which are associated with DYT16, a rare form of dystonia-parkinsonism. Dystonia is a movement disorder that causes muscles to contract involuntarily, leading to repetitive movements or abnormal postures. Parkinsonism refers to a group of conditions that share some of the symptoms of Parkinson’s disease, such as tremors, slowness, and stiffness.

DYT16 is a particularly rare genetic disorder, and its diagnosis is crucial for understanding the specific challenges it presents and exploring appropriate treatment options. The test is conducted through a blood sample or cheek swab, analyzing the genetic makeup to detect any abnormalities in the PRKRA gene that could indicate the presence of DYT16.

DNA Labs UAE offers this test at a cost of 4400 AED. By providing this service, DNA Labs UAE facilitates early and accurate diagnosis, which is essential for managing symptoms and improving the quality of life for individuals affected by this disorder. This test is a critical step for families seeking answers to unexplained symptoms of dystonia and parkinsonism, offering hope through personalized medicine and targeted therapies based on genetic information.

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
Guaranteed Safe Checkout

PRKRA Gene DYT16 Genetic Test

Test Name: PRKRA Gene DYT16 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Clinical History of Patient who is going for PRKRA Gene DYT16 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKRA Gene DYT16.

Test Details: The PRKRA gene is associated with a rare movement disorder known as DYT16 dystonia. This disorder causes involuntary muscle contractions and spasms, leading to abnormal movements and postures. NGS (next-generation sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of DYT16 dystonia, an NGS genetic test can identify variations or mutations in the PRKRA gene that may be responsible for the disorder. If a person is suspected to have DYT16 dystonia, an NGS genetic test may be recommended by a healthcare provider to confirm the diagnosis. This can help guide treatment options and provide important information for family members who may be at risk for the disorder.

Test Name PRKRA Gene DYT16 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 PRKRA Gene DYT16 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRKRA Gene DYT16
Test Details

The PRKRA gene is associated with a rare movement disorder known as DYT16 dystonia. This disorder causes involuntary muscle contractions and spasms, leading to abnormal movements and postures.

NGS (next-generation sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of DYT16 dystonia, an NGS genetic test can identify variations or mutations in the PRKRA gene that may be responsible for the disorder.

If a person is suspected to have DYT16 dystonia, an NGS genetic test may be recommended by a healthcare provider to confirm the diagnosis. This can help guide treatment options and provide important information for family members who may be at risk for the disorder.