CCT5 Gene Neuropathy hereditary sensory with spastic paraplegia Genetic Test
At DNA Labs UAE, we offer the CCT5 Gene Neuropathy hereditary sensory with spastic paraplegia Genetic Test at a cost of AED 4400.0. This test is designed to analyze the CCT5 gene for mutations associated with hereditary sensory neuropathy with spastic paraplegia.
Test Components and Price
Test Name: CCT5 Gene Neuropathy hereditary sensory with spastic paraplegia Genetic Test
Price: AED 4400.0
Sample Condition
Sample can be either Blood, Extracted DNA, or One drop Blood on FTA Card.
Report Delivery
Reports are typically delivered within 3 to 4 weeks.
Method
The test utilizes NGS (Next-Generation Sequencing) technology.
Test Type
This test is specifically designed for Neurological Disorders.
Doctor
The test is conducted by a Neurologist.
Test Department
The test is conducted in our Genetics department.
Pre Test Information
Prior to the test, it is recommended to provide the clinical history of the patient who is going for the CCT5 Gene Neuropathy test. Additionally, a Genetic Counselling session is conducted to draw a pedigree chart of family members affected with CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia.
Test Details
The CCT5 Gene Neuropathy hereditary sensory with spastic paraplegia Genetic Test is a genetic test that analyzes the CCT5 gene for mutations associated with hereditary sensory neuropathy with spastic paraplegia. This condition is characterized by progressive sensory loss in the limbs, muscle weakness and stiffness (spasticity) in the lower limbs, and other neurological symptoms.
NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes. In the context of this genetic test, NGS is used to identify any variations or mutations in the CCT5 gene that may be causing or contributing to the symptoms of hereditary sensory neuropathy with spastic paraplegia.
By identifying specific genetic mutations, this test can help confirm a diagnosis, provide information about disease prognosis and progression, guide treatment decisions, and offer valuable information for genetic counseling and family planning.
| Test Name | CCT5 Gene Neuropathy hereditary sensory with spastic paraplegia 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 CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia |
| Test Details |
CCT5 Gene Neuropathy, hereditary sensory, with spastic paraplegia NGS Genetic Test is a genetic test that analyzes the CCT5 gene for mutations associated with hereditary sensory neuropathy with spastic paraplegia. This condition is characterized by progressive sensory loss in the limbs, muscle weakness and stiffness (spasticity) in the lower limbs, and other neurological symptoms. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes. In the context of this genetic test, NGS is used to identify any variations or mutations in the CCT5 gene that may be causing or contributing to the symptoms of hereditary sensory neuropathy with spastic paraplegia. By identifying specific genetic mutations, this test can help confirm a diagnosis, provide information about disease prognosis and progression, guide treatment decisions, and offer valuable information for genetic counseling and family planning. |
