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PRICKLE2 Gene Epilepsy progressive myoclonic type 5 Genetic Test

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

-21%

The PRICKLE2 Gene Epilepsy Progressive Myoclonic Type 5 Genetic Test is a specialized diagnostic assessment conducted at DNA Labs UAE. This test is designed to identify mutations in the PRICKLE2 gene, which have been associated with Progressive Myoclonic Epilepsy type 5 (EPM5). EPM5 is a rare genetic disorder characterized by myoclonus, seizures, and, in some cases, progressive neurological decline. The identification of mutations in the PRICKLE2 gene through this test is crucial for accurate diagnosis, which can significantly influence management and treatment strategies for affected individuals. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze genetic material for the specific mutations linked to this form of epilepsy. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect reliable and actionable genetic insights that can help in tailoring individualized care plans.

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PRICKLE2 Gene Epilepsy progressive myoclonic type 5 Genetic Test

Test Details

The PRICKLE2 gene is associated with a rare form of epilepsy known as progressive myoclonic epilepsy type 5 (EPM5). This genetic disorder is characterized by seizures, muscle jerks (myoclonus), and progressive neurological deterioration.

NGS (Next-Generation Sequencing) is a genetic testing method that can identify mutations or changes in the DNA sequence of the PRICKLE2 gene that may be responsible for EPM5. This test involves analyzing the patient’s DNA sample to detect any variations in the gene that could be causing the disorder.

Genetic testing for EPM5 can help diagnose the condition and provide information on the specific genetic mutation that is causing the disorder. This can help guide treatment options and provide information for family planning. However, genetic testing is not always necessary for the diagnosis of EPM5 and should be discussed with a healthcare provider.

Test Name: PRICKLE2 Gene Epilepsy progressive myoclonic type 5 Genetic 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: Clinical History of Patient who is going for PRICKLE2 Gene Epilepsy, progressive myoclonic type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRICKLE2 Gene Epilepsy, progressive myoclonic type 5.

For more information or to schedule a genetic test, please contact DNA Labs UAE.

Test Name PRICKLE2 Gene Epilepsy progressive myoclonic type 5 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 PRICKLE2 Gene Epilepsy, progressive myoclonic type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRICKLE2 Gene Epilepsy, progressive myoclonic type 5
Test Details

The PRICKLE2 gene is associated with a rare form of epilepsy known as progressive myoclonic epilepsy type 5 (EPM5). This genetic disorder is characterized by seizures, muscle jerks (myoclonus), and progressive neurological deterioration.

NGS (Next-Generation Sequencing) is a genetic testing method that can identify mutations or changes in the DNA sequence of the PRICKLE2 gene that may be responsible for EPM5. This test involves analyzing the patient’s DNA sample to detect any variations in the gene that could be causing the disorder.

Genetic testing for EPM5 can help diagnose the condition and provide information on the specific genetic mutation that is causing the disorder. This can help guide treatment options and provide information for family planning. However, genetic testing is not always necessary for the diagnosis of EPM5 and should be discussed with a healthcare provider.