EIF2B2 Gene Leukoencephalopathy with vanishing white matter Genetic Test sale cost 4400 AED
HPRT1 Gene Lesch-Nyham syndrome Genetic Test sale cost 4400 AED HPRT1 Gene Lesch-Nyham syndrome Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
SGCA Gene Limb-girdle muscular dystrophy autosomal recessive type 2D Genetic Test sale cost 4400 AED SGCA Gene Limb-girdle muscular dystrophy autosomal recessive type 2D Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

EIF2B2 Gene Leukoencephalopathy with vanishing white matter Genetic Test Cost

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

-21%

The EIF2B2 gene plays a critical role in the regulation of protein synthesis within cells and is particularly significant in the context of neurological development and function. Mutations in this gene are associated with leukoencephalopathy with vanishing white matter (VWM), a rare and progressive condition characterized by the deterioration of white matter in the brain. This deterioration leads to symptoms such as spasticity, ataxia, seizures, and cognitive decline, typically triggered or worsened by febrile infections or minor head trauma.

To diagnose this condition, genetic testing for mutations in the EIF2B2 gene, among others, is crucial. DNA Labs UAE offers a comprehensive genetic test targeting the EIF2B2 gene to confirm the diagnosis of leukoencephalopathy with vanishing white matter. This test is essential for individuals displaying symptoms of VWM, or for families with a history of the condition seeking a definitive diagnosis.

The test is priced at 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the EIF2B2 gene. Conducted in a state-of-the-art laboratory by experienced geneticists, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific genetic alterations known to cause VWM.

This genetic test not only facilitates an accurate diagnosis but also helps in understanding the progression of the disease, informing treatment decisions, and providing essential information for family planning. Given the complexity and rarity of VWM, access to such precise genetic testing at DNA Labs UAE represents a critical step forward for affected individuals and their families, offering hope for better management and understanding of the condition.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

EIF2B2 Gene Leukoencephalopathy with vanishing white matter Genetic Test

Test Name: EIF2B2 Gene Leukoencephalopathy with vanishing white matter 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 EIF2B2 Gene Leukoencephalopathy with vanishing white matter NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EIF2B2 Gene Leukoencephalopathy with vanishing white matter.

Test Details

The EIF2B2 gene is associated with a rare genetic disorder called Leukoencephalopathy with vanishing white matter (VWM). This disorder affects the white matter of the brain, leading to neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes. In the context of Leukoencephalopathy with vanishing white matter, NGS genetic testing can be used to identify mutations or variations in the EIF2B2 gene that may be responsible for the development of the disorder.

By analyzing the DNA sequence of the EIF2B2 gene, NGS genetic testing can provide information about any genetic changes or mutations present in the gene. This information can help diagnose individuals with VWM and provide valuable information for genetic counseling and family planning.

It is important to note that NGS genetic testing is a complex process and should be performed by trained professionals in a specialized laboratory setting. The results of the test should be interpreted by a healthcare professional familiar with the specific genetic disorder and its implications.

Test Name EIF2B2 Gene Leukoencephalopathy with vanishing white matter 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 EIF2B2 Gene Leukoencephalopathy with vanishing white matter NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with EIF2B2 Gene Leukoencephalopathy with vanishing white matter
Test Details

The EIF2B2 gene is associated with a rare genetic disorder called Leukoencephalopathy with vanishing white matter (VWM). This disorder affects the white matter of the brain, leading to neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes. In the context of Leukoencephalopathy with vanishing white matter, NGS genetic testing can be used to identify mutations or variations in the EIF2B2 gene that may be responsible for the development of the disorder.

By analyzing the DNA sequence of the EIF2B2 gene, NGS genetic testing can provide information about any genetic changes or mutations present in the gene. This information can help diagnose individuals with VWM and provide valuable information for genetic counseling and family planning.

It is important to note that NGS genetic testing is a complex process and should be performed by trained professionals in a specialized laboratory setting. The results of the test should be interpreted by a healthcare professional familiar with the specific genetic disorder and its implications.

SKU: TEST-1518 Category:

Related products