MYH7B Gene Cardiomyopathy Left Ventricular Noncompaction Genetic Test
Are you or a family member at risk of MYH7B gene cardiomyopathy and left ventricular noncompaction? DNA Labs UAE offers a comprehensive genetic test to detect mutations in the MYH7B gene, providing crucial information for diagnosis, prognosis, and treatment decisions.
Test Details
MYH7B gene cardiomyopathy is a genetic disorder that affects the heart muscle, resulting in the development of cardiomyopathy. Cardiomyopathy refers to a group of diseases that weaken and enlarge the heart muscle, impairing its ability to effectively pump blood. Left ventricular noncompaction (LVNC) is a specific type of cardiomyopathy characterized by excessive trabeculations (spongy-like structures) in the left ventricle of the heart. These trabeculations can hinder the pumping function of the heart and increase the risk of heart failure, arrhythmias, and blood clots.
The MYH7B gene is associated with LVNC and provides instructions for producing a protein called myosin heavy chain 7B. This protein is essential for the contraction of heart muscle cells. Mutations in the MYH7B gene can disrupt the normal function of the protein, leading to the development of LVNC.
NGS Genetic Testing
NGS (Next-Generation Sequencing) genetic testing is a cutting-edge technique that allows for the simultaneous analysis of multiple genes, enabling the identification of mutations or variations in their sequences. In the context of MYH7B-related LVNC, an NGS genetic test can be performed to examine the MYH7B gene for disease-causing mutations.
Test Components
- Test Name: MYH7B Gene Cardiomyopathy Left Ventricular Noncompaction MYH7B related Genetic Test
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Cardiovascular Pneumology Disorders
- Doctor: Cardiologist
- Test Department: Genetics
Pre Test Information
Before undergoing the MYH7B Gene Cardiomyopathy Left Ventricular Noncompaction Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to create a pedigree chart of family members affected by MYH7B Gene Cardiomyopathy, left ventricular noncompaction, and MYH7B related NGS Genetic DNA Test gene MYH7B.
Benefits of Genetic Testing
The MYH7B Gene Cardiomyopathy Left Ventricular Noncompaction Genetic Test offers several benefits:
- Confirmation of diagnosis
- Information about disease progression
- Assessment of the risk of complications
- Guidance for treatment decisions
Genetic Testing Guidance
It is crucial to undergo genetic testing under the guidance of a healthcare professional or genetic counselor. These experts can provide appropriate counseling and interpretation of the test results, ensuring the best possible care and understanding for patients and their families.
Test Name | MYH7B Gene Cardiomyopathy left ventricular noncompaction MYH7B related Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Cardiovascular Pneumology Disorders |
Doctor | Cardiologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for MYH7B Gene Cardiomyopathy, left ventricular noncompaction, MYH7B related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYH7B Gene Cardiomyopathy, left ventricular noncompaction, MYH7B related NGS Genetic DNA Test gene MYH7B |
Test Details |
MYH7B gene cardiomyopathy is a genetic disorder that affects the heart muscle, leading to the development of cardiomyopathy. Cardiomyopathy refers to a group of diseases that weaken and enlarge the heart muscle, making it harder for the heart to pump blood effectively. Left ventricular noncompaction (LVNC) is a specific type of cardiomyopathy characterized by the presence of excessive trabeculations (spongy-like structures) in the left ventricle of the heart. These trabeculations can impair the pumping function of the heart and increase the risk of heart failure, arrhythmias, and blood clots. The MYH7B gene is one of the genes associated with LVNC. It provides instructions for making a protein called myosin heavy chain 7B, which is involved in the contraction of heart muscle cells. Mutations in the MYH7B gene can disrupt the normal function of the protein, leading to the development of LVNC. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify mutations or variations in their sequences. In the context of MYH7B-related LVNC, an NGS genetic test can be performed to examine the MYH7B gene for any disease-causing mutations. This test helps in confirming the diagnosis, providing information about disease progression, assessing the risk of complications, and guiding treatment decisions. It is important to note that genetic testing should be carried out under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results. |