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TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test Cost

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

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The TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the TDP1 gene, which are implicated in the development of spinocerebellar ataxia with axonal neuropathy. This condition is a rare, inherited neurological disorder characterized by a progressive loss of muscle coordination (ataxia) and nerve damage (neuropathy), affecting movement and sensory functions. The test is crucial for individuals with a family history of the disorder or those exhibiting symptoms, providing essential information for accurate diagnosis and management. Priced at 4400 AED, this genetic test involves analyzing the patient’s DNA to detect specific mutations in the TDP1 gene, helping in confirming the diagnosis and guiding treatment options, while also offering the possibility for family planning and genetic counseling for affected families.

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TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test

Welcome to DNA Labs UAE, where we offer the TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test. This test is designed to detect the presence of mutations or variations in the TDP1 gene, which is associated with a condition called spinocerebellar ataxia with axonal neuropathy. This condition is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene to develop the condition.

The cost of the TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test is 4400.0 AED. The test can be performed using a blood sample, extracted DNA, or one drop of blood on an FTA card. The results of the test will be delivered within 3 to 4 weeks.

The TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of genetic testing, NGS can be used to analyze the entire coding region of the TDP1 gene to identify any mutations or variations that may be associated with spinocerebellar ataxia with axonal neuropathy.

This genetic test is specifically designed to diagnose spinocerebellar ataxia with axonal neuropathy, provide information about disease progression and prognosis, and guide treatment decisions. It can also be useful for family planning and genetic counseling, as it can determine carrier status in individuals who may be at risk of passing on the condition to their children.

Prior to undergoing the TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test, it is recommended to provide the clinical history of the patient and participate in a genetic counseling session. This session will involve drawing a pedigree chart of family members affected with spinocerebellar ataxia with axonal neuropathy, autosomal recessive.

If you suspect that you or a loved one may be affected by spinocerebellar ataxia with axonal neuropathy, we encourage you to consult with a neurologist who specializes in neurological disorders. Our test is performed in our Genetics department, ensuring accurate and reliable results.

By undergoing the TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive Genetic Test, you can gain valuable insights into your condition, make informed decisions about your treatment, and plan for the future. Contact DNA Labs UAE today to schedule your test and take control of your health.

Test Name TDP1 Gene Spinocerebellar ataxia with axonal neuropathy autosomal recessive 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 TDP1 Gene Spinocerebellar ataxia with axonal neuropathy, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TDP1 Gene Spinocerebellar ataxia with axonal neuropathy, autosomal recessive
Test Details

The TDP1 gene is associated with a condition called spinocerebellar ataxia with axonal neuropathy, which is inherited in an autosomal recessive manner. Autosomal recessive means that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of genetic testing, NGS can be used to analyze the entire coding region of the TDP1 gene to identify any mutations or variations that may be associated with spinocerebellar ataxia with axonal neuropathy.

Genetic testing for spinocerebellar ataxia with axonal neuropathy can help confirm a diagnosis, provide information about disease progression and prognosis, and guide treatment decisions. It can also be useful for family planning and genetic counseling, as it can determine carrier status in individuals who may be at risk of passing on the condition to their children.

SKU: TEST-2084 Category:

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