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Dystonia Gene Panel Test

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

The Dystonia Gene Panel Test, available at DNA Labs UAE, is a sophisticated diagnostic tool designed to identify genetic mutations associated with dystonia, a complex neurological movement disorder. This condition is characterized by involuntary muscle contractions, leading to repetitive movements or abnormal postures. Dystonia can affect just one muscle, a group of muscles, or muscles throughout the body, and it can be a primary condition or a symptom of another disease.

The test, which costs 7200 AED, involves analyzing a comprehensive panel of genes known to be linked to various forms of dystonia. By examining a patient’s DNA, the test aims to pinpoint specific genetic abnormalities that may be causing or contributing to the disorder. This targeted approach not only aids in confirming a diagnosis of dystonia but also helps in understanding the type and potential severity of the condition. Furthermore, the results can guide treatment decisions, assist in predicting the course of the disease, and provide valuable information for family planning.

DNA Labs UAE employs state-of-the-art genetic testing technology to ensure accurate and reliable results. The test is performed under strict quality controls and is interpreted by experts in genetics and neurology. For individuals exhibiting symptoms of dystonia or those with a family history of the disorder, the Dystonia Gene Panel Test offers a crucial step towards achieving a clearer understanding of their condition and exploring appropriate treatment options.

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Dystonia Gene Panel Test – Cost AED 7200.0

Welcome to DNA Labs UAE, a leading genetic laboratory in the UAE. In this blog post, we will discuss the Dystonia Gene Panel Test, its cost, symptoms, diagnosis, and other important details.

Test Name: Dystonia Gene Panel Test

Components:

  • Sterile container
  • Sterile Normal Saline Container
  • EDTA Vacutainer

Price: 7200.0 AED

Sample Condition:

The Dystonia Gene Panel Test can be performed using the following sample conditions:

  • Amniotic fluid
  • Chorionic villi
  • Peripheral blood

Report Delivery: 4-6 weeks

Method: NGS (Next-Generation Sequencing)

Test Type: Genetics

Doctor: General Physician

Test Department:

Pre Test Information:

The Dystonia Gene Panel Test requires a doctor’s prescription. However, please note that the prescription is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.

Test Details:

The Dystonia Gene Panel Test is a genetic test that analyzes multiple genes associated with dystonia. Dystonia is a movement disorder characterized by involuntary muscle contractions that cause repetitive or twisting movements. The panel typically includes genes such as TOR1A, THAP1, and GCH1, among others.

This test can help identify the underlying genetic cause of dystonia in individuals and their family members. It plays a crucial role in diagnosis, treatment, and genetic counseling. The test is usually ordered by a healthcare provider and involves a blood or saliva sample. The results are typically interpreted by a genetic counselor or medical specialist.

Test Name Dystonia Gene Panel Test
Components Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer
Price 7200.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi\/ Peripheral blood
Report Delivery 4-6 weeks
Method NGS
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Dystonia Gene Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The Dystonia Gene Panel is a genetic test that analyzes multiple genes associated with dystonia, a movement disorder characterized by involuntary muscle contractions that cause repetitive or twisting movements. The panel typically includes genes such as TOR1A, THAP1, and GCH1, among others. The test can help identify the underlying genetic cause of dystonia in individuals and their family members, which can aid in diagnosis, treatment, and genetic counseling. The test is usually ordered by a healthcare provider and involves a blood or saliva sample. Results are typically interpreted by a genetic counselor or medical specialist.