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RTN2 Gene SPG12 Genetic Test

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

-21%

The RTN2 gene SPG12 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the RTN2 gene, which are linked to spastic paraplegia 12 (SPG12), a rare form of hereditary spastic paraplegia. This condition is characterized by progressive weakness and stiffness of the legs, which can lead to severe mobility issues and other neurological complications. The test involves analyzing the patient’s DNA to detect any genetic abnormalities that may be responsible for the condition.

Performed at DNA Labs UAE, a leading facility in genetic testing, the RTN2 gene SPG12 genetic test is conducted with high precision and accuracy, utilizing advanced genomic technologies. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the expertise required to interpret the results. This test is crucial for individuals with a family history of hereditary spastic paraplegia or those exhibiting symptoms, as it can provide a definitive diagnosis, inform treatment strategies, and offer insights into the risk of passing the condition onto future generations.

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RTN2 Gene SPG12 Genetic Test

Cost: 4400.0 AED

Test Components

  • 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

Clinical History of Patient who is going for RTN2 Gene SPG12 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with RTN2 Gene SPG12

Test Details

The RTN2 gene is associated with hereditary spastic paraplegia type 12 (SPG12), which is a neurodegenerative disorder characterized by progressive muscle stiffness and weakness in the lower limbs.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of variations or mutations in specific genes, such as the RTN2 gene, which may be responsible for causing or contributing to a particular genetic disorder like SPG12.

NGS genetic testing for the RTN2 gene in individuals suspected of having SPG12 can help confirm the diagnosis and identify the specific genetic mutation responsible for the condition. This information can be used for genetic counseling, family planning, and potentially targeted treatment strategies in the future.

Test Name RTN2 Gene SPG12 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 RTN2 Gene SPG12 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with RTN2 Gene SPG12
Test Details

The RTN2 gene is associated with hereditary spastic paraplegia type 12 (SPG12), which is a neurodegenerative disorder characterized by progressive muscle stiffness and weakness in the lower limbs.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of variations or mutations in specific genes, such as the RTN2 gene, which may be responsible for causing or contributing to a particular genetic disorder like SPG12.

NGS genetic testing for the RTN2 gene in individuals suspected of having SPG12 can help confirm the diagnosis and identify the specific genetic mutation responsible for the condition. This information can be used for genetic counseling, family planning, and potentially targeted treatment strategies in the future.

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