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WASHC5 Gene SPG8 Genetic Test Cost

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

-21%

The WASHC5 Gene SPG8 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the WASHC5 gene, which are associated with Spastic Paraplegia 8 (SPG8). SPG8 is a rare genetic disorder characterized by progressive weakness and spasticity of the lower limbs. Early and accurate detection through this genetic test can be crucial for the management and treatment of the condition. The test involves collecting a DNA sample from the patient, which is then analyzed for specific genetic alterations in the WASHC5 gene that are indicative of SPG8. DNA Labs UAE provides this comprehensive genetic testing service for a cost of 4400 AED. This test is essential for individuals with a family history of SPG8 or those exhibiting symptoms, as it can offer critical insights into their condition and guide healthcare professionals in developing an effective treatment plan.

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WASHC5 Gene SPG8 Genetic Test

At DNA Labs UAE, we offer the WASHC5 Gene SPG8 Genetic Test for individuals suspected of having hereditary spastic paraplegia (HSP). HSP is a neurodegenerative disorder characterized by progressive weakness and stiffness in the lower limbs, making walking difficult. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously to identify variations or mutations in the WASHC5 gene that may be responsible for causing HSP.

Test Components and Price

The WASHC5 Gene SPG8 Genetic Test is priced at 4400.0 AED. The test can be performed on blood samples, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

After the test is conducted, the report will be delivered within 3 to 4 weeks.

Test Method

The WASHC5 Gene SPG8 Genetic Test utilizes NGS technology to analyze the DNA sequence of the WASHC5 gene.

Test Type and Doctor

The test falls under the category of Neurological Disorders and is conducted by a Neurologist in our Genetics department.

Pre Test Information

Prior to the test, a Genetic Counselling session is conducted to gather the clinical history of the patient and draw a pedigree chart of family members affected with WASHC5 Gene SPG8.

Test Details

The WASHC5 gene, also known as KIAA0196 or SPG8, is associated with hereditary spastic paraplegia (HSP). HSP is a progressive neurodegenerative disorder characterized by weakness and stiffness in the lower limbs. NGS genetic testing allows us to detect variations or mutations in the WASHC5 gene that may be responsible for causing HSP.

By analyzing the DNA sequence of the WASHC5 gene, NGS testing can confirm a diagnosis of SPG8 in individuals suspected of having the condition. It can also provide information about the specific genetic variant or mutation present, which is valuable for understanding the underlying cause of the disease and for genetic counseling purposes.

It is important to note that genetic testing for SPG8 is recommended for individuals with symptoms suggestive of HSP and a family history of the condition. The test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate guidance and counseling based on the test results.

Test Name WASHC5 Gene SPG8 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 WASHC5 Gene SPG8 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with WASHC5 Gene SPG8
Test Details

The WASHC5 gene, also known as KIAA0196 or SPG8, is associated with a hereditary neurodegenerative disorder called hereditary spastic paraplegia (HSP). HSP is characterized by progressive weakness and stiffness in the lower limbs, leading to difficulty in walking and sometimes other neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify variations or mutations that may be associated with a particular condition. In the case of SPG8, NGS genetic testing can be used to detect variations or mutations in the WASHC5 gene that may be responsible for causing HSP.

By analyzing the DNA sequence of the WASHC5 gene, NGS testing can help confirm a diagnosis of SPG8 in individuals suspected of having the condition. It can also provide information about the specific genetic variant or mutation present, which can be helpful for understanding the underlying cause of the disease and for genetic counseling purposes.

It is important to note that genetic testing for SPG8 is typically recommended for individuals with symptoms suggestive of HSP and a family history of the condition. The test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate guidance and counseling based on the test results.

SKU: TEST-2036 Category:

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