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GABRB3 Gene Epilepsy childhood absence type 5 Genetic Test

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

-21%

The GABRB3 gene plays a crucial role in the development and function of the brain, particularly in the regulation of neurotransmission. Mutations in this gene have been linked to various neurological conditions, including Epilepsy Childhood Absence Type 5 (ECAT5). This specific type of epilepsy is characterized by frequent absence seizures that begin in childhood, significantly affecting attention and learning.

To diagnose and manage ECAT5 effectively, genetic testing for mutations in the GABRB3 gene is essential. DNA Labs UAE offers a comprehensive genetic test designed to identify mutations in the GABRB3 gene that are associated with Epilepsy Childhood Absence Type 5. This test is a valuable tool for clinicians in confirming the diagnosis, which can then guide treatment decisions and genetic counseling.

The cost of the GABRB3 gene epilepsy genetic test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the GABRB3 gene. The results of this test can provide crucial information for the effective management and treatment of individuals with ECAT5, offering them a better quality of life.

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GABRB3 Gene Epilepsy Childhood Absence Type 5 Genetic Test

Test Name: GABRB3 Gene Epilepsy Childhood Absence Type 5 Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GABRB3 Gene Epilepsy, Childhood Absence Type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GABRB3 Gene Epilepsy, Childhood Absence Type 5.

Test Details

The GABRB3 gene is associated with epilepsy, specifically childhood absence type 5. Childhood absence epilepsy is a type of seizure disorder that typically begins in early childhood and is characterized by brief episodes of staring or loss of awareness.

NGS genetic testing can identify mutations or variations in the GABRB3 gene that may contribute to the development of childhood absence epilepsy. This type of testing involves sequencing the DNA in the GABRB3 gene to look for any abnormalities that may be causing the disorder.

Knowing whether a person has a mutation or variation in the GABRB3 gene can help with diagnosis and treatment of childhood absence epilepsy. It can also provide information about the risk of passing the condition on to future generations.

It is important to note that genetic testing is not always necessary or appropriate for every person with childhood absence epilepsy. A healthcare provider can help determine if genetic testing is necessary and provide counseling about the potential benefits and risks of testing.

Test Name GABRB3 Gene Epilepsy childhood absence 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 GABRB3 Gene Epilepsy, childhood absence type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GABRB3 Gene Epilepsy, childhood absence type 5
Test Details

The GABRB3 gene is associated with epilepsy, specifically childhood absence type 5. Childhood absence epilepsy is a type of seizure disorder that typically begins in early childhood and is characterized by brief episodes of staring or loss of awareness.

NGS genetic testing can identify mutations or variations in the GABRB3 gene that may contribute to the development of childhood absence epilepsy. This type of testing involves sequencing the DNA in the GABRB3 gene to look for any abnormalities that may be causing the disorder.

Knowing whether a person has a mutation or variation in the GABRB3 gene can help with diagnosis and treatment of childhood absence epilepsy. It can also provide information about the risk of passing the condition on to future generations.

It is important to note that genetic testing is not always necessary or appropriate for every person with childhood absence epilepsy. A healthcare provider can help determine if genetic testing is necessary and provide counseling about the potential benefits and risks of testing.