CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 Genetic Test sale cost 4400 AED
KCNQ1 Gene Short QT Syndrome Type 2 Genetic Test sale cost 4400 AED KCNQ1 Gene Short QT Syndrome Type 2 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Pneumonia Plus Advantage Test sale cost 4870 AED Pneumonia Plus Advantage Test Cost 5,410 د.إ Original price was: 5,410 د.إ.4,870 د.إCurrent price is: 4,870 د.إ.
Sale!

CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 Genetic Test Cost

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

-21%

The CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE. This test is designed to detect mutations in the CALM1 gene, which are linked to Catecholaminergic Polymorphic Ventricular Tachycardia Type 4 (CPVT4), a rare but potentially life-threatening genetic disorder. CPVT4 is characterized by an abnormal heart rhythm (ventricular tachycardia) that occurs in response to physical activity or emotional stress, leading to fainting spells, seizures, or even sudden death if left undiagnosed and untreated.

The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the CALM1 gene. Identifying these mutations can help in confirming the diagnosis of CPVT4, enabling personalized treatment plans that can significantly reduce the risk of cardiac events.

The cost of the CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 Genetic Test at DNA Labs UAE is 4400 AED. Given the critical nature of the condition it tests for, this test is an essential tool for individuals with a family history of CPVT or unexplained syncopal episodes, providing them with the opportunity for early intervention and management of the condition.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 Genetic Test

Components: CALM1 Gene Ventricular Tachycardia Catecholaminergic Polymorphic Type 4 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: Clinical History of Patient who is going for CALM1 Gene Ventricular Tachycardia, Catecholaminergic Polymorphic Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CALM1 Gene Ventricular Tachycardia, Catecholaminergic Polymorphic Type 4 NGS Genetic DNA Test gene CALM1

Test Details: The CALM1 gene is a gene that codes for the calmodulin protein, which is involved in regulating calcium signaling in cells. Mutations in the CALM1 gene have been associated with various cardiac conditions, including ventricular tachycardia. Ventricular tachycardia is a type of abnormal heart rhythm characterized by rapid and irregular electrical signals in the ventricles, the lower chambers of the heart. It can be life-threatening if not properly managed. Catecholaminergic polymorphic ventricular tachycardia type 4 (CPVT4) is a specific subtype of ventricular tachycardia that is caused by mutations in the CALM1 gene. It is an inherited condition that is typically triggered by physical activity or emotional stress. CPVT4 can be diagnosed through genetic testing, specifically Next-Generation Sequencing (NGS) Genetic Testing. NGS Genetic Testing is a method that allows for the simultaneous sequencing of multiple genes in a single test. It enables the detection of genetic mutations associated with various conditions, including CPVT4. This type of testing can provide valuable information for diagnosis, prognosis, and treatment decisions. If a person has a family history of ventricular tachycardia or other cardiac conditions, or if they have experienced unexplained episodes of rapid heart rate, their healthcare provider may recommend NGS Genetic Testing to check for mutations in the CALM1 gene or other relevant genes associated with ventricular tachycardia. It is important to note that genetic testing should always be conducted and interpreted by qualified healthcare professionals who specialize in genetics and cardiovascular diseases. They can provide appropriate counseling, explain the results, and guide patients and their families in making informed decisions regarding their healthcare.

Test Name CALM1 Gene Ventricular tachycardia catecholaminergic polymorphic type 4 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 CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic DNA Test gene CALM1
Test Details

The CALM1 gene is a gene that codes for the calmodulin protein, which is involved in regulating calcium signaling in cells. Mutations in the CALM1 gene have been associated with various cardiac conditions, including ventricular tachycardia.

Ventricular tachycardia is a type of abnormal heart rhythm characterized by rapid and irregular electrical signals in the ventricles, the lower chambers of the heart. It can be life-threatening if not properly managed.

Catecholaminergic polymorphic ventricular tachycardia type 4 (CPVT4) is a specific subtype of ventricular tachycardia that is caused by mutations in the CALM1 gene. It is an inherited condition that is typically triggered by physical activity or emotional stress. CPVT4 can be diagnosed through genetic testing, specifically Next-Generation Sequencing (NGS) Genetic Testing.

NGS Genetic Testing is a method that allows for the simultaneous sequencing of multiple genes in a single test. It enables the detection of genetic mutations associated with various conditions, including CPVT4. This type of testing can provide valuable information for diagnosis, prognosis, and treatment decisions.

If a person has a family history of ventricular tachycardia or other cardiac conditions, or if they have experienced unexplained episodes of rapid heart rate, their healthcare provider may recommend NGS Genetic Testing to check for mutations in the CALM1 gene or other relevant genes associated with ventricular tachycardia.

It is important to note that genetic testing should always be conducted and interpreted by qualified healthcare professionals who specialize in genetics and cardiovascular diseases. They can provide appropriate counseling, explain the results, and guide patients and their families in making informed decisions regarding their healthcare.

SKU: TEST-3492 Category:

Related products