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ACTG2 Gene Visceral Myopathy Genetic Test

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

-21%

The ACTG2 Gene Visceral Myopathy Genetic Test is a specialized diagnostic procedure designed to identify mutations in the ACTG2 gene, which are associated with visceral myopathy. Visceral myopathy is a rare condition that affects the smooth muscles of the gastrointestinal tract, leading to severe digestive issues and complications. This genetic test is a critical tool for confirming the diagnosis, understanding the disease’s progression, and guiding treatment decisions for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the ACTG2 gene to detect any genetic abnormalities that may contribute to the condition. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing techniques to identify mutations.

The cost of the ACTG2 Gene Visceral Myopathy Genetic Test is 4400 AED. While the price may seem high, the test provides invaluable insights into the genetic underpinnings of visceral myopathy, enabling targeted interventions and personalized care plans. For families and individuals facing the challenges of visceral myopathy, this genetic test represents a crucial step toward better management of the condition and improved quality of life.

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ACTG2 Gene Visceral Myopathy Genetic Test

At DNA Labs UAE, we offer the ACTG2 Gene Visceral Myopathy Genetic Test at a cost of AED 4400.0. This test is used to diagnose visceral myopathy, a rare genetic disorder that affects the smooth muscle cells in the gastrointestinal tract.

Test Details

The ACTG2 gene is responsible for producing a protein called actin gamma-2 smooth muscle, which is primarily found in smooth muscle cells. These cells are present in various organs throughout the body, including the digestive tract, blood vessels, and airways.

Visceral myopathy can cause a range of symptoms, such as difficulty swallowing, constipation, diarrhea, and abdominal pain. To accurately diagnose this condition, we use NGS (Next-Generation Sequencing) technology, which allows us to analyze multiple genes simultaneously.

During the test, we sequence the ACTG2 gene to identify any genetic variants or mutations that may be causing or contributing to visceral myopathy. This information can help in the diagnosis of the condition and guide treatment and management decisions.

Test Components and Price

– Test Name: ACTG2 Gene Visceral Myopathy Genetic Test

– Components: Blood Sample

– Price: AED 4400.0

Report Delivery

After the sample is collected, it takes approximately 3 to 4 weeks for the test results to be processed and the report to be delivered to the doctor.

Test Type and Department

– Test Type: Dysmorphology

– Doctor: Pediatrics

– Test Department: Genetics

Pre-Test Information

Prior to the ACTG2 Gene Visceral Myopathy Genetic Test, it is important to provide the clinical history of the patient who is undergoing the test. Additionally, a genetic counseling session may be conducted to create a pedigree chart of family members affected by ACTG2 Gene Visceral Myopathy NGS Genetic DNA Test gene ACTG2.

By gathering this information, we can gain a better understanding of the patient’s genetic background and family history, which can aid in the interpretation of the test results.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. If you suspect that you or your child may have visceral myopathy, we encourage you to consult with a doctor and consider the ACTG2 Gene Visceral Myopathy Genetic Test.

Test Name ACTG2 Gene Visceral myopathy Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ACTG2 Gene Visceral myopathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTG2 Gene Visceral myopathy NGS Genetic DNA Test gene ACTG2
Test Details

The ACTG2 gene is responsible for providing instructions to make a protein called actin gamma-2 smooth muscle, which is primarily found in smooth muscle cells. These cells are found in various organs throughout the body, including the digestive tract, blood vessels, and airways.

Visceral myopathy is a rare genetic disorder that affects the smooth muscle cells in the gastrointestinal tract. It can lead to a variety of symptoms, including difficulty swallowing, constipation, diarrhea, and abdominal pain.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to analyze multiple genes simultaneously. It can provide a comprehensive evaluation of a person’s genetic makeup and identify any genetic variants or mutations that may be associated with a particular condition, such as visceral myopathy.

Therefore, an ACTG2 gene NGS genetic test would involve sequencing the ACTG2 gene to look for any genetic variants or mutations that may be causing or contributing to visceral myopathy. This test can help in the diagnosis of the condition and provide information about the specific genetic changes involved, which can be helpful for treatment and management decisions.