CASQ2 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 2 Genetic Test
Welcome to DNA Labs UAE, a leading genetic laboratory in the UAE. We offer the CASQ2 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 2 Genetic Test to diagnose and detect symptoms of this rare inherited cardiac disorder.
Test Components and Price
Test Name: CASQ2 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 2 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery
Report Delivery Time: 3 to 4 Weeks
Method
Method: NGS Technology (Next-Generation Sequencing)
Test Type
Test Type: Cardiovascular Pneumology Disorders
Doctor and Test Department
Doctor: Cardiologist
Test Department: Genetics
Pre Test Information
Before undergoing the CASQ2 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 2 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 the CASQ2 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 2 NGS Genetic DNA Test gene CASQ2.
Test Details
The CASQ2 gene is associated with a condition called catecholaminergic polymorphic ventricular tachycardia type 2 (CPVT2). CPVT is a rare inherited cardiac disorder characterized by an abnormal heart rhythm called ventricular tachycardia. This condition is typically triggered by physical activity or emotional stress.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. It uses high-throughput sequencing technologies to rapidly sequence large amounts of DNA or RNA. In the context of CPVT2, NGS genetic testing can be used to identify mutations or variations in the CASQ2 gene that may be responsible for the condition.
By identifying specific genetic variants in the CASQ2 gene, NGS genetic testing can help confirm a diagnosis of CPVT2 in individuals with suspected or confirmed symptoms. It can also be used for genetic counseling and to inform family members about their risk of inheriting the condition.
It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics or cardiovascular medicine. They can provide appropriate counseling and interpretation of the test results.
| Test Name | CASQ2 Gene Ventricular tachycardia catecholaminergic polymorphic type 2 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 CASQ2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASQ2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 2 NGS Genetic DNA Test gene CASQ2 |
| Test Details | The CASQ2 gene is associated with a condition called catecholaminergic polymorphic ventricular tachycardia type 2 (CPVT2). CPVT is a rare inherited cardiac disorder characterized by an abnormal heart rhythm called ventricular tachycardia. This condition is typically triggered by physical activity or emotional stress. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. It uses high-throughput sequencing technologies to rapidly sequence large amounts of DNA or RNA. In the context of CPVT2, NGS genetic testing can be used to identify mutations or variations in the CASQ2 gene that may be responsible for the condition. By identifying specific genetic variants in the CASQ2 gene, NGS genetic testing can help confirm a diagnosis of CPVT2 in individuals with suspected or confirmed symptoms. It can also be used for genetic counseling and to inform family members about their risk of inheriting the condition. It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics or cardiovascular medicine. They can provide appropriate counseling and interpretation of the test results. |
