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AP4S1 Gene SPG52 Genetic Test Cost

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

-21%

The AP4S1 gene SPG52 genetic test is a specialized diagnostic procedure designed to detect mutations in the AP4S1 gene, which are linked to Spastic Paraplegia 52 (SPG52). SPG52 is a rare genetic disorder characterized by progressive weakness and stiffness of the legs, part of a group of disorders known as hereditary spastic paraplegias. These mutations can lead to various neurological symptoms, including developmental delay, intellectual disability, and problems with movement and coordination.

Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, this test is pivotal for early diagnosis and management of SPG52. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the AP4S1 gene. The results can provide valuable information for affected individuals and their families, including insights into the condition’s progression, potential treatments, and the risk of passing the disorder to future generations.

The cost of the AP4S1 gene SPG52 genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive analysis and expertise required to accurately identify mutations in the AP4S1 gene and provide a conclusive diagnosis. For families and individuals facing the possibility of SPG52, this test represents a crucial step towards understanding and managing the condition.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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AP4S1 Gene SPG52 Genetic Test

At DNA Labs UAE, we offer the AP4S1 Gene SPG52 Genetic Test for individuals suspected of having hereditary spastic paraplegia (HSP). This rare neurodegenerative disorder is characterized by progressive weakness and stiffness in the legs, resulting in difficulty walking.

Test Details

The AP4S1 gene, also known as SPG52, is associated with HSP. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, helping us identify genetic variations that may be responsible for causing HSP.

Components and Price

The cost of the AP4S1 Gene SPG52 Genetic Test is 4400.0 AED. We accept blood or extracted DNA samples, or even just one drop of blood 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 AP4S1 Gene SPG52 Genetic Test falls under the category of Neurological Disorders and is conducted by our Genetics department.

Pre Test Information

Prior to the test, we require a clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by AP4S1 Gene SPG52.

Doctor and Method

The test will be conducted by a Neurologist using NGS technology.

Importance of Genetic Testing

Genetic testing can help confirm a diagnosis, understand disease progression, and provide appropriate genetic counseling and management for individuals and their families affected by HSP. However, it is crucial that genetic testing is performed and interpreted by qualified healthcare professionals specializing in genetics and neurology.

Genetic Counseling

We strongly recommend genetic counseling both before and after the test. This will allow individuals to discuss the potential risks, benefits, and limitations of testing, as well as the implications of the results for themselves and their families.

Test Name AP4S1 Gene SPG52 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 AP4S1 Gene SPG52 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with AP4S1 Gene SPG52
Test Details

AP4S1 gene, also known as SPG52, is associated with a rare neurodegenerative disorder called hereditary spastic paraplegia (HSP). HSP is characterized by progressive weakness and stiffness in the legs, leading to difficulty in walking. It is caused by the degeneration of nerve fibers that control muscle movement in the lower limbs.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify genetic variations that may be associated with a specific disorder or condition. In the case of AP4S1/SPG52 gene, NGS genetic testing can help identify mutations or variations in this gene that may be responsible for causing HSP.

By analyzing the AP4S1 gene using NGS, healthcare professionals can determine whether a person has genetic variations in this gene that are associated with HSP. This information can be helpful in confirming a diagnosis, understanding disease progression, and providing appropriate genetic counseling and management for individuals and their families affected by HSP.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who specialize in genetics and neurology. Genetic counseling is also recommended before and after genetic testing to discuss the potential risks, benefits, and limitations of testing, as well as the implications of the results for the individual and their family.

SKU: TEST-2016 Category:

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