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ACTB Gene Dystonia Juvenile-Onset Genetic Test

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

-21%

The ACTB Gene Dystonia Juvenile-Onset Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the ACTB gene that are associated with the early onset of dystonia. Dystonia is a movement disorder characterized by involuntary muscle contractions, leading to repetitive movements or abnormal postures. The ACTB gene plays a crucial role in the production of beta-actin, a protein essential for cell structure and integrity, and mutations in this gene can disrupt normal muscle function and lead to dystonia.

This genetic test is particularly important for individuals showing symptoms of dystonia at a young age, as early detection can significantly impact the management and treatment options available. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the ACTB gene that are known to cause juvenile-onset dystonia.

DNA Labs UAE offers this comprehensive genetic test at a cost of 4400 AED. The test not only aids in the accurate diagnosis of dystonia but also helps in understanding the genetic predisposition of the condition, enabling families to make informed decisions regarding future family planning. The results from this test can also provide valuable information for personalized treatment plans, improving the quality of life for those affected by this challenging condition.

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ACTB Gene Dystonia Juvenile-Onset Genetic Test

Welcome to DNA Labs UAE, where we offer the ACTB Gene Dystonia Juvenile-Onset Genetic Test. This test is designed to diagnose and analyze the genetic mutations associated with juvenile-onset dystonia, a condition that causes involuntary muscle contractions and abnormal postures. Read on to learn more about this test and its components.

Test Name: ACTB Gene Dystonia Juvenile-Onset Genetic Test

  • Components: Genetic analysis of the ACTB gene
  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 2 to 4 Weeks
  • Method: NGS Technology (Next-Generation Sequencing)
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the ACTB Gene Dystonia Juvenile-Onset Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by juvenile-onset dystonia.

Test Details

The ACTB gene is associated with juvenile-onset dystonia, a condition that typically begins in childhood or adolescence. It manifests through involuntary muscle contractions and abnormal postures. Our NGS genetic testing method allows us to analyze the patient’s DNA and identify any genetic mutations or variations in the ACTB gene that may contribute to the development of the condition.

NGS testing involves taking a small sample of blood or saliva from the patient. This sample is then analyzed using specialized equipment and software. The results of the test provide valuable insights to doctors and genetic counselors, enabling them to better understand the patient’s condition and develop personalized treatment plans.

It is important to note that genetic testing is not always necessary or appropriate for every patient with dystonia. The decision to undergo genetic testing should be made in consultation with a healthcare provider or genetic counselor who can assess the potential benefits and risks of the test.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. If you suspect juvenile-onset dystonia or have any concerns about your genetic health, consult with our experienced neurologist and genetics team today.

Test Name ACTB Gene Dystonia juvenile-onset Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 263 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 ACTB Gene Dystonia juvenile-onset NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ACTB Gene Dystonia juvenile-onset
Test Details

The ACTB gene is associated with a type of dystonia called juvenile-onset dystonia. This condition typically begins in childhood or adolescence and causes involuntary muscle contractions and abnormal postures.

NGS (next-generation sequencing) genetic testing is a method used to analyze a person’s DNA to identify genetic mutations or variations that may be associated with a particular condition. In the case of juvenile-onset dystonia, NGS testing can be used to identify mutations in the ACTB gene that may be contributing to the development of the condition.

NGS testing typically involves taking a small sample of blood or saliva from the patient and analyzing the DNA in the sample using specialized equipment and software. The results of the test can help doctors and genetic counselors to better understand the patient’s condition and develop personalized treatment plans.

It is important to note that genetic testing is not always necessary or appropriate for every patient with dystonia. The decision to undergo genetic testing should be made in consultation with a healthcare provider or genetic counselor who can help assess the potential benefits and risks of the test.

SKU: TEST-1255 Category:

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