Sale!

PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test

4,400 د.إ

-21%

The PLCB1 gene plays a crucial role in brain development and function. Mutations in this gene have been linked to early infantile epileptic encephalopathy type 12 (EIEE12), a severe neurological disorder. This condition is characterized by early-onset seizures, developmental delay, and sometimes other neurological complications. Genetic testing for mutations in the PLCB1 gene is essential for diagnosing EIEE12, guiding treatment options, and providing genetic counseling for affected families.

At DNA Labs UAE, a specialized genetic test is available for identifying mutations in the PLCB1 gene associated with early infantile epileptic encephalopathy type 12. The test involves analyzing the patient’s DNA to detect specific genetic alterations that cause the condition. This precise genetic testing is a crucial step in the diagnosis and management of EIEE12, allowing for tailored treatment plans and support for patients and their families.

The cost of the PLCB1 gene test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis necessary to identify the genetic underpinnings of EIEE12, providing invaluable information for affected individuals and their healthcare providers. Through this testing, DNA Labs UAE offers hope and direction for families navigating the challenges of early infantile epileptic encephalopathy type 12.

Home  Sample collection service available

  • 100% accuaret DNA Results
  • Ranked as Most trusted Genetic DNA Lab
Guaranteed Safe Checkout

PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test

Are you looking for a reliable genetic lab in UAE to conduct the PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test? Look no further than DNA Labs UAE. Our state-of-the-art lab offers accurate and efficient genetic testing services at an affordable cost.

Test Details

The PLCB1 gene is associated with early infantile epileptic encephalopathy type 12 (EIEE12), a rare genetic disorder characterized by seizures that begin in infancy. Our NGS genetic test for EIEE12 involves sequencing the PLCB1 gene to identify any mutations or variations that may be causing the disorder.

This test is crucial for diagnosis, prognosis, and treatment planning for individuals with EIEE12. It provides valuable insights into the genetic makeup of the patient, allowing healthcare providers and genetic counselors to develop personalized treatment plans.

It is important to note that genetic testing for EIEE12 should always be done under the guidance of a healthcare provider or genetic counselor. Our team of experienced neurologists and geneticists will ensure that the test is conducted accurately and the results are interpreted correctly.

Test Components and Price

Our PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test is priced at 4400.0 AED. The test requires either a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test results will be delivered within 3 to 4 weeks after the sample is received in our lab. We understand the importance of timely results, and our team works diligently to provide accurate and comprehensive reports as quickly as possible.

Test Method

We utilize NGS (Next-Generation Sequencing) technology for our PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test. NGS is a cutting-edge technology that allows for faster and more accurate sequencing of genes, enabling us to identify mutations or variations with high precision.

Test Type and Department

The PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test falls under the category of Neurological Disorders. It is conducted by our dedicated Genetics department, which comprises experienced geneticists and technicians.

Pre Test Information

Prior to conducting the PLCB1 Gene Early infantile epileptic encephalopathy type 12 NGS Genetic DNA Test, we require the clinical history of the patient. This information helps us better understand the patient’s condition and ensures accurate interpretation of the test results.

We also recommend a Genetic Counselling session to draw a pedigree chart of family members affected with PLCB1 Gene Early infantile epileptic encephalopathy type 12. This session helps us assess the genetic inheritance pattern and identify potential carriers of the disorder within the family.

Choose DNA Labs UAE for Reliable Genetic Testing

At DNA Labs UAE, we prioritize accuracy, efficiency, and patient satisfaction. Our team of highly skilled professionals is dedicated to providing top-notch genetic testing services, including the PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test.

By choosing us, you can rest assured that your genetic test will be conducted using state-of-the-art technology and interpreted by experienced neurologists and geneticists. We understand the importance of genetic testing in guiding diagnosis and treatment decisions, and we strive to deliver accurate and reliable results.

Don’t wait any longer. Contact DNA Labs UAE today to schedule your PLCB1 Gene Early infantile epileptic encephalopathy type 12 Genetic Test and take a step towards personalized and effective healthcare.

Test Name PLCB1 Gene Early infantile epileptic encephalopathy type 12 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 PLCB1 Gene Early infantile epileptic encephalopathy type 12 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PLCB1 Gene Early infantile epileptic encephalopathy type 12
Test Details

The PLCB1 gene is associated with early infantile epileptic encephalopathy type 12 (EIEE12), which is a rare genetic disorder characterized by seizures that begin in infancy. The NGS genetic test for EIEE12 involves sequencing the PLCB1 gene to identify any mutations or variations that may be causing the disorder. This test can help with diagnosis, prognosis, and treatment planning for individuals with EIEE12. It is important to note that genetic testing for EIEE12 should be done under the guidance of a healthcare provider or genetic counselor.