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GABRG2 Gene Epilepsy childhood absence type 2 Genetic Test

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

-21%

The GABRG2 gene is associated with a form of epilepsy known as childhood absence epilepsy type 2, a condition characterized by frequent, brief loss of consciousness and staring spells. This condition often starts in childhood and can significantly impact an individual’s quality of life. The GABRG2 gene plays a crucial role in the functioning of GABA receptors, which are involved in inhibiting nerve transmission in the brain, and mutations in this gene can disrupt this process, leading to seizures.

DNA Labs UAE offers a specialized genetic test to identify mutations in the GABRG2 gene, which can be instrumental in diagnosing childhood absence epilepsy type 2. This test is particularly valuable for families with a history of this condition, providing them with crucial information that can guide treatment and management strategies. The test is priced at 4400 AED and involves a simple procedure, typically requiring only a blood sample or cheek swab from the patient.

By identifying specific genetic mutations associated with epilepsy, this test enables healthcare providers to offer a more personalized approach to treatment, potentially improving outcomes for affected individuals. It also offers families the opportunity to understand their risk of passing the condition onto future generations, aiding in informed family planning decisions.

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GABRG2 Gene Epilepsy Childhood Absence Type 2 Genetic Test

At DNA Labs UAE, we offer the GABRG2 Gene Epilepsy Childhood Absence Type 2 Genetic Test for individuals who suspect they may have this condition. Our test can provide valuable information on diagnosis and risk factors, helping patients make informed decisions about their health.

Test Name: GABRG2 Gene Epilepsy Childhood Absence Type 2 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 GABRG2 Gene Epilepsy, childhood absence type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GABRG2 Gene Epilepsy, childhood absence type 2

Test Details

The GABRG2 gene is associated with the development of epilepsy, specifically childhood absence type 2 epilepsy. This type of epilepsy is characterized by sudden and brief episodes of staring or loss of consciousness, typically lasting less than 20 seconds.

NGS (next-generation sequencing) genetic testing can be used to analyze the GABRG2 gene for mutations or variations that may be linked to childhood absence type 2 epilepsy. This type of testing can help diagnose the condition and provide information on the risk of passing it on to future generations.

It is important to note that genetic testing alone is not always sufficient for a diagnosis of epilepsy. Clinical evaluation and other diagnostic tests may also be necessary.

Test Name GABRG2 Gene Epilepsy childhood absence type 2 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 GABRG2 Gene Epilepsy, childhood absence type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GABRG2 Gene Epilepsy, childhood absence type 2
Test Details

The GABRG2 gene is associated with the development of epilepsy, specifically childhood absence type 2 epilepsy. This type of epilepsy is characterized by sudden and brief episodes of staring or loss of consciousness, typically lasting less than 20 seconds.

NGS (next-generation sequencing) genetic testing can be used to analyze the GABRG2 gene for mutations or variations that may be linked to childhood absence type 2 epilepsy. This type of testing can help diagnose the condition and provide information on the risk of passing it on to future generations.

It is important to note that genetic testing alone is not always sufficient for a diagnosis of epilepsy. Clinical evaluation and other diagnostic tests may also be necessary.