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NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test Cost

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

-21%

The “NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test” is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the NKX2-5 gene. This gene plays a crucial role in the development of the heart, and mutations within it can lead to congenital heart defects, such as atrial septal defects (ASDs) and atrioventricular (AV) conduction defects. ASDs are characterized by an opening in the wall between the two upper chambers of the heart, while AV conduction defects affect the electrical system that controls the heartbeat, potentially leading to arrhythmias.

The test is particularly valuable for individuals with a clinical diagnosis of these conditions or those with a family history, aiding in the accurate diagnosis and guiding appropriate management and treatment strategies. It involves the collection of a DNA sample, typically through a blood draw, which is then analyzed for specific genetic alterations in the NKX2-5 gene that are known to be associated with these cardiac anomalies.

The cost of the test at DNA Labs UAE is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it offers into the patient’s condition. This testing not only facilitates early detection and intervention for affected individuals but also provides critical information for family planning and genetic counseling for families with a history of these congenital heart defects.

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NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test

At DNA Labs UAE, we offer the NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test. This test helps in diagnosing individuals with atrial septal defect and atrioventricular conduction defects. The test is performed using NGS (Next-Generation Sequencing) technology, which allows for a comprehensive analysis of an individual’s genetic makeup.

Test Details

The NKX2-5 gene is responsible for producing a protein called homeobox protein Nkx-2.5, which plays a crucial role in the development and function of the heart. Atrial septal defect (ASD) is a congenital heart defect characterized by an abnormal opening in the wall that separates the two upper chambers of the heart. This opening allows blood to flow between the atria, leading to various complications.

Atrioventricular conduction defects refer to abnormalities in the electrical conduction system of the heart, which can disrupt the coordination of the heart’s contractions. By analyzing the NKX2-5 gene through NGS genetic testing, we can identify any genetic variations or mutations that may be associated with these conditions.

Test Components and Price

The NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test costs AED 4400.0. The test can be performed using blood or extracted DNA, or just one drop of blood on an FTA card.

Report Delivery and Method

Once the test is performed, the report will be delivered within 3 to 4 weeks. The method used for this test is NGS technology, which allows for a comprehensive analysis of multiple genes simultaneously.

Test Type and Doctor

The NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test falls under the category of dysmorphology. This test is recommended for pediatric patients and is conducted by our team of experienced pediatric doctors.

Test Department and Pre-Test Information

The test is conducted in our Genetics department. Before undergoing the NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects 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 these conditions.

Conclusion

The NKX2-5 Gene Atrial Septal Defect with Atrioventricular Conduction Defects Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing individuals with atrial septal defect and atrioventricular conduction defects. Through NGS genetic testing, we can identify any genetic variations or mutations in the NKX2-5 gene, allowing for personalized treatment and management strategies. If you suspect that you or your family members may be affected by these conditions, we encourage you to consider this genetic test.

Test Name NKX2-5 Gene Atrial septal defect with atrioventricular conduction defects 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for NKX2-5 Gene Atrial septal defect with atrioventricular conduction defects NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NKX2-5 Gene Atrial septal defect with atrioventricular conduction defects NGS Genetic DNA Test gene NKX2-5
Test Details

The NKX2-5 gene is a gene that provides instructions for making a protein called homeobox protein Nkx-2.5. This protein is involved in the development and function of the heart.

Atrial septal defect (ASD) is a congenital heart defect where there is an abnormal opening in the wall that separates the two upper chambers of the heart (atria). This opening allows blood to flow between the atria, which can lead to various complications.

Atrioventricular conduction defects refer to abnormalities in the electrical conduction system of the heart, which can cause problems with the coordination of the heart’s contractions.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the context of the NKX2-5 gene, NGS genetic testing can be used to identify any genetic variations or mutations in the NKX2-5 gene that may be associated with atrial septal defect and atrioventricular conduction defects.

By identifying these genetic variations, NGS genetic testing can help in diagnosing individuals with these conditions, predicting the risk of developing these conditions in family members, and guiding personalized treatment and management strategies.