SPG11 Gene SPG11 Genetic Test
At DNA Labs UAE, we offer the SPG11 Gene SPG11 Genetic Test for individuals who are experiencing symptoms consistent with hereditary spastic paraplegia (HSP) type 11. This rare neurodegenerative disorder is characterized by progressive muscle weakness and stiffness in the legs, which can make walking difficult.
Test Details
The SPG11 Gene SPG11 Genetic Test utilizes NGS (next-generation sequencing) technology, which allows us to analyze multiple genes simultaneously. By examining the SPG11 gene, we can identify any mutations or changes that may be causing the disorder.
Components and Price
The cost of the SPG11 Gene SPG11 Genetic Test is AED 4400.0. The test requires a blood sample or extracted DNA, or 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 SPG11 Gene SPG11 Genetic Test falls under the category of neurological disorders and is conducted by our Genetics department.
Pre Test Information
Prior to the test, we recommend a genetic counseling session to gather clinical history and draw a pedigree chart of family members affected by SPG11 Gene SPG11. This will help us better understand the genetic inheritance pattern within the family.
Why Choose Genetic Testing for SPG11?
Genetic testing for SPG11 is essential for confirming a diagnosis and determining the specific genetic cause of the condition. It can also help identify carriers of the SPG11 gene mutation within a family and provide genetic counseling to individuals at risk of passing the condition on to their children.
It’s important to note that genetic testing for SPG11 is typically only recommended for individuals who have symptoms consistent with hereditary spastic paraplegia and a suspected genetic cause. The test is usually ordered by a healthcare provider or genetic counselor who specializes in genetic disorders.
At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. If you suspect SPG11 may be the cause of your symptoms, consult with a neurologist or genetic counselor to discuss the possibility of undergoing the SPG11 Gene SPG11 Genetic Test.
| Test Name | SPG11 Gene SPG11 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 SPG11 Gene SPG11 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SPG11 Gene SPG11 |
| Test Details |
The SPG11 gene is associated with a rare neurodegenerative disorder called hereditary spastic paraplegia type 11 (SPG11). This condition is characterized by progressive muscle weakness and stiffness in the legs (spastic paraplegia), which can eventually lead to difficulty walking. NGS (next-generation sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of SPG11, NGS genetic testing can identify mutations or changes in the SPG11 gene that may be causing the disorder. This type of genetic testing can be helpful in confirming a diagnosis of SPG11 and determining the specific genetic cause of the condition. It can also be useful for identifying carriers of the SPG11 gene mutation within a family and providing genetic counseling to individuals at risk of passing the condition on to their children. It’s important to note that genetic testing for SPG11 is typically only recommended for individuals who have symptoms consistent with hereditary spastic paraplegia and a suspected genetic cause. The test is usually ordered by a healthcare provider or genetic counselor who specializes in genetic disorders. |
