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KCNA2 Gene Early infantile epileptic encephalopathy type 32 Genetic Test Cost

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

-21%

The KCNA2 gene early infantile epileptic encephalopathy type 32 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the KCNA2 gene, which are associated with early infantile epileptic encephalopathy type 32 (EIEE32). This condition is a severe form of epilepsy that manifests in the first few months of life, characterized by frequent seizures and significant developmental delays. The test plays a crucial role in the early detection and management of this condition, allowing for tailored treatment plans that can improve the quality of life for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient’s DNA to look for specific genetic alterations in the KCNA2 gene that are linked to EIEE32. This state-of-the-art lab ensures accurate and reliable results, leveraging advanced genetic sequencing technologies.

The cost of the KCNA2 gene early infantile epileptic encephalopathy type 32 genetic test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive process of sample collection, DNA extraction, sequencing, and expert analysis, providing families with crucial information regarding the genetic underpinnings of the condition. Early diagnosis through this test can significantly impact the management strategies for affected infants, paving the way for interventions that can mitigate the severity of symptoms and promote better developmental outcomes.

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KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 Genetic Test

At DNA Labs UAE, we offer the KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 Genetic Test. This test is designed to diagnose individuals with early infantile epileptic encephalopathy type 32 (EIEE32), a rare genetic disorder characterized by seizures that begin in infancy.

Test Details

The KCNA2 gene is associated with EIEE32. This disorder is caused by mutations in the KCNA2 gene, which provides instructions for making a protein called a voltage-gated potassium channel. This channel helps regulate the flow of charged particles (ions) in and out of cells in the brain and other tissues.

Our NGS genetic test for EIEE32 involves analyzing the DNA sequence of the KCNA2 gene to identify mutations or changes that may be causing the disorder. This type of test can help diagnose EIEE32 in individuals with symptoms of the disorder and can also be used to identify carriers of KCNA2 mutations in families with a history of the disorder.

Early diagnosis and genetic testing can help guide treatment and management of EIEE32. By identifying the specific genetic mutation causing the disorder, healthcare professionals can develop personalized treatment plans for patients.

Test Components and Price

The KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks. Our team of experts will thoroughly analyze the genetic data to provide accurate and reliable results.

Referring Doctor and Test Department

The KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 Genetic Test is recommended by neurologists specializing in neurological disorders. The test is conducted in our Genetics department.

Pre-Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32.

Genetic counseling can help individuals and their families understand the inheritance pattern of the disorder and make informed decisions about family planning and potential treatment options.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 Genetic Test can help diagnose this rare genetic disorder and guide treatment decisions. Contact us today to learn more or schedule a test.

Test Name KCNA2 Gene Early infantile epileptic encephalopathy type 32 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 KCNA2 Gene Early infantile epileptic encephalopathy type 32 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KCNA2 Gene Early infantile epileptic encephalopathy type 32
Test Details

The KCNA2 gene is associated with early infantile epileptic encephalopathy type 32 (EIEE32), a rare genetic disorder characterized by seizures that begin in infancy. The disorder is caused by mutations in the KCNA2 gene, which provides instructions for making a protein called a voltage-gated potassium channel. This channel helps regulate the flow of charged particles (ions) in and out of cells in the brain and other tissues.

A NGS genetic test for EIEE32 involves analyzing the DNA sequence of the KCNA2 gene to identify mutations or changes that may be causing the disorder. This type of test can help diagnose EIEE32 in individuals with symptoms of the disorder and can also be used to identify carriers of KCNA2 mutations in families with a history of the disorder. Early diagnosis and genetic testing can help guide treatment and management of EIEE32.

SKU: TEST-1299 Category:

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