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CSTB Gene Unverricht-Lundborg Disease Genetic Test Cost

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

-21%

The CSTB gene Unverricht-Lundborg Disease genetic test is a specialized diagnostic tool used to detect mutations in the CSTB gene, which are responsible for causing Unverricht-Lundborg Disease (ULD) – a rare type of inherited epilepsy. This autosomal recessive genetic disorder is characterized by myoclonic seizures, tonic-clonic seizures, and in some cases, cognitive decline. Early detection through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The laboratory then analyzes the sample to identify any mutations in the CSTB gene that are indicative of Unverricht-Lundborg Disease. The accuracy of this test makes it a valuable resource for families with a history of the condition, offering them an opportunity for early intervention and genetic counseling.

The cost of the CSTB gene Unverricht-Lundborg Disease genetic test at DNA Labs UAE is 4400 AED. Given the specialized nature of this test and the advanced technology used in the analysis, the price reflects the comprehensive approach taken to ensure accurate and reliable results. For patients and families facing the challenges of Unverricht-Lundborg Disease, this test represents a crucial step towards effective management and treatment of the condition.

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  • This test is not intended for medical diagnosis or treatment
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CSTB Gene Unverricht-Lundborg disease Genetic Test

At DNA Labs UAE, we offer the CSTB Gene Unverricht-Lundborg disease Genetic Test for individuals who suspect they may have Unverricht-Lundborg disease (ULD). This test focuses on the CSTB gene, which is associated with ULD, a progressive myoclonic epilepsy disorder characterized by sudden muscle jerks or twitches.

Test Components and Price

The CSTB Gene Unverricht-Lundborg disease Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes Next-Generation Sequencing (NGS) technology, which allows for the rapid and efficient sequencing of large amounts of genetic material.

Test Type and Doctor

The CSTB Gene Unverricht-Lundborg disease Genetic Test falls under the category of Neurological Disorders. It is conducted by our experienced neurologists in the Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the CSTB Gene Unverricht-Lundborg disease NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by ULD.

Test Details

The CSTB gene Unverricht-Lundborg disease NGS genetic test focuses on analyzing specific regions of the CSTB gene to identify disease-causing mutations or variations. This information is crucial in confirming a diagnosis of ULD and providing insights into the specific genetic variant responsible for the disease.

NGS technology plays a significant role in this test, allowing for the efficient sequencing of genetic material. The results obtained from this test can be utilized for genetic counseling, family planning, and potentially for the development of targeted therapies in the future.

Test Name CSTB Gene Unverricht-Lundborg disease 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 CSTB Gene Unverricht-Lundborg disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CSTB Gene Unverricht-Lundborg disease
Test Details

CSTB gene Unverricht-Lundborg disease NGS genetic test is a type of genetic test that focuses on the CSTB gene to diagnose Unverricht-Lundborg disease (ULD). ULD is an inherited neurological disorder characterized by progressive myoclonic epilepsy, which causes sudden, brief muscle jerks or twitches.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the rapid and efficient sequencing of large amounts of genetic material. In the context of the CSTB gene ULD genetic test, NGS is used to analyze the specific regions of the CSTB gene to identify any disease-causing mutations or variations.

By detecting mutations in the CSTB gene, this genetic test can help confirm a diagnosis of ULD and provide information about the specific genetic variant causing the disease. This information can be valuable for genetic counseling, family planning, and potentially for the development of targeted therapies in the future.

SKU: TEST-2101