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B4GALNT1 Gene SPG26 Genetic Test Cost

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

-21%

The B4GALNT1 Gene SPG26 Genetic Test is a specialized diagnostic tool designed to detect mutations in the B4GALNT1 gene, which are associated with Spastic Paraplegia 26 (SPG26), a rare neurodegenerative disorder. This condition is characterized by progressive weakness and spasticity of the lower limbs, and it falls under the category of hereditary spastic paraplegias. The test is particularly crucial for individuals showing symptoms of the disease or those with a family history of SPG26, as it can provide definitive genetic evidence of the condition.

Conducted at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services, the test involves analyzing the patient’s DNA to identify any mutations in the B4GALNT1 gene that might lead to the disorder. The process is meticulous and requires a sample of the patient’s blood or saliva, from which DNA is extracted and examined for the specific genetic changes.

The cost of the B4GALNT1 Gene SPG26 Genetic Test at DNA Labs UAE is set at 4400 AED. While this may represent a significant investment, the value of the test lies in its ability to provide individuals and families with crucial information regarding the genetic basis of SPG26, facilitating informed decisions about treatment options and management of the disorder. It also aids in genetic counseling for affected families, offering insights into the risk of passing the condition to future generations.

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
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B4GALNT1 Gene SPG26 Genetic Test

At DNA Labs UAE, we offer the B4GALNT1 Gene SPG26 Genetic Test to help diagnose and understand hereditary spastic paraplegia type 26 (SPG26). This rare genetic disorder is characterized by progressive muscle stiffness and weakness in the lower limbs.

Test Details

The B4GALNT1 gene is associated with SPG26. To analyze this gene, we use NGS (Next-Generation Sequencing) technology. NGS allows for the rapid and cost-effective sequencing of large portions of the genome, including the B4GALNT1 gene, to identify any genetic variations or mutations that may be causing SPG26.

Test Components and Price

The cost of the B4GALNT1 Gene SPG26 Genetic Test is AED 4400.0. The test can be performed on blood or extracted DNA samples. Alternatively, one drop of blood can be collected on an FTA Card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Test Type and Department

The B4GALNT1 Gene SPG26 Genetic Test falls under the category of Neurological Disorders. The test is conducted by our experienced Neurologist in the Genetics department.

Pre Test Information

Before undergoing the B4GALNT1 Gene SPG26 NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with B4GALNT1 Gene SPG26.

This information is crucial for accurate diagnosis, genetic counseling, and potentially guiding treatment options for individuals with SPG26.

Test Name B4GALNT1 Gene SPG26 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 B4GALNT1 Gene SPG26 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with B4GALNT1 Gene SPG26
Test Details

The B4GALNT1 gene is associated with hereditary spastic paraplegia type 26 (SPG26), which is a rare genetic disorder characterized by progressive muscle stiffness and weakness in the lower limbs.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput method used to analyze multiple genes simultaneously. It allows for the rapid and cost-effective sequencing of large portions of the genome, including the B4GALNT1 gene, to identify any genetic variations or mutations that may be causing SPG26.

By performing an NGS genetic test on the B4GALNT1 gene, healthcare professionals can determine if there are any specific genetic changes or mutations present that may be responsible for the development of SPG26. This information can be crucial for accurate diagnosis, genetic counseling, and potentially guiding treatment options for individuals with SPG26.

SKU: TEST-1998 Category:

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