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STXBP1 Gene Early infantile epileptic encephalopathy type 4 Genetic Test

4,400 د.إ

-21%

The STXBP1 gene is associated with early infantile epileptic encephalopathy type 4 (EIEE4), a severe neurological disorder characterized by early-onset seizures and developmental delays. Genetic testing for mutations in the STXBP1 gene is crucial for diagnosing this condition, enabling early intervention and personalized management strategies for affected individuals.

DNA Labs UAE offers a comprehensive genetic test targeting the STXBP1 gene to identify mutations that may lead to EIEE4. The test is designed to provide accurate and reliable results, which are essential for the diagnosis and treatment planning of this epileptic encephalopathy. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed.

By opting for this genetic test, families and healthcare providers can gain valuable insights into the genetic underpinnings of the condition, facilitating informed decisions about care and support for those affected by EIEE4.

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STXBP1 Gene Early Infantile Epileptic Encephalopathy Type 4 Genetic Test

Welcome to DNA Labs UAE, where we offer the STXBP1 Gene Early Infantile Epileptic Encephalopathy Type 4 Genetic Test. This test is designed to analyze the STXBP1 gene for mutations that may cause Early Infantile Epileptic Encephalopathy Type 4 (EIEE4), a rare genetic disorder characterized by seizures, developmental delays, and intellectual disability.

Test Details

The STXBP1 gene is associated with Early Infantile Epileptic Encephalopathy Type 4 (EIEE4). Our NGS (Next-Generation Sequencing) genetic testing method involves sequencing the entire gene and analyzing any variations or mutations in the DNA sequence.

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

Before undergoing the STXBP1 Gene Early Infantile Epileptic Encephalopathy Type 4 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by STXBP1 Gene Early Infantile Epileptic Encephalopathy Type 4.

Treatment and Genetic Counseling

Early diagnosis through genetic testing can greatly assist in the management and treatment of EIEE4. Treatment options may include medications to control seizures and developmental therapies to improve cognitive and motor skills. Genetic counseling may also be recommended for families affected by EIEE4 to discuss the risks and inheritance patterns of the disorder.

Test Name STXBP1 Gene Early infantile epileptic encephalopathy type 4 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 STXBP1 Gene Early infantile epileptic encephalopathy type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with STXBP1 Gene Early infantile epileptic encephalopathy type 4
Test Details

The STXBP1 gene is associated with Early Infantile Epileptic Encephalopathy Type 4 (EIEE4), which is a rare genetic disorder characterized by seizures that begin in the first months of life, developmental delays, and intellectual disability.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the STXBP1 gene for mutations that may cause EIEE4. This test involves sequencing the entire gene and analyzing any variations or mutations in the DNA sequence.

Early diagnosis through genetic testing can help in the management and treatment of the disorder. Treatment options may include medications to control seizures and developmental therapies to improve cognitive and motor skills. Genetic counseling may also be recommended for families affected by EIEE4 to discuss the risks and inheritance patterns of the disorder.