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GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test Cost

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

-21%

The GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, aimed at identifying mutations in the GATA4 gene which are associated with Ventricular Septal Defect Type 1 (VSD1). This condition is a congenital heart defect characterized by a hole in the wall separating the heart’s lower chambers, affecting the flow of blood within the heart. The GATA4 gene plays a crucial role in heart development and function, and mutations in this gene can lead to various cardiac anomalies including VSD1.

The test is particularly recommended for individuals with a clinical diagnosis of ventricular septal defect, those with a family history of congenital heart defects, or prospective parents with concerns about genetic inheritance of heart conditions. It involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the GATA4 gene.

The cost of the GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive analysis and the use of advanced genetic testing technologies to provide accurate and reliable results. The test offers valuable insights for affected individuals and their families, aiding in the understanding of the genetic basis of the condition, informing clinical management, and guiding decision-making regarding treatment options and family planning.

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  • This test is not intended for medical diagnosis or treatment
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GATA4 Gene Ventricular septal defect type 1 Genetic Test

At DNA Labs UAE, we offer the GATA4 Gene Ventricular septal defect type 1 Genetic Test for individuals who may be at risk of developing ventricular septal defect type 1 (VSD1). This genetic test can provide valuable information about the presence of genetic mutations or variants that may be associated with this congenital heart defect.

Test Details

The GATA4 gene is responsible for producing a protein called GATA-binding protein 4, which plays a crucial role in heart development during embryonic stages. VSD1 is a type of congenital heart defect characterized by a hole in the wall that separates the ventricles of the heart. This hole allows oxygen-rich blood from the left ventricle to mix with oxygen-poor blood from the right ventricle.

Our GATA4 Gene Ventricular septal defect type 1 Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the sequencing of multiple genes or even the entire genome simultaneously. By analyzing the GATA4 gene using NGS technology, we can identify any genetic mutations or variants that may be associated with VSD1.

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

Prior to undergoing the GATA4 Gene Ventricular septal defect type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by VSD1 and the GATA4 gene. This information can help in understanding the inheritance pattern and potential risk factors associated with the condition.

Benefits of the Test

The GATA4 Gene Ventricular septal defect type 1 NGS Genetic Test can provide several benefits:

  • Diagnosis: The test can aid in diagnosing ventricular septal defect type 1 and confirming the presence of genetic mutations or variants.
  • Genetic Understanding: By identifying the genetic basis of VSD1, individuals and their families can gain a better understanding of the condition and its potential implications.
  • Risk Identification: The test can help identify individuals who may be at risk of developing ventricular septal defect type 1, allowing for early intervention and preventive measures.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our GATA4 Gene Ventricular septal defect type 1 Genetic Test can provide valuable insights into the genetic factors associated with VSD1. Contact us today to schedule an appointment or learn more about our services.

Test Name GATA4 Gene Ventricular septal defect type 1 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 GATA4 Gene Ventricular septal defect type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GATA4 Gene Ventricular septal defect type 1 NGS Genetic DNA Test gene GATA4
Test Details

The GATA4 gene is a gene that provides instructions for making a protein called GATA-binding protein 4. This protein is involved in the development of the heart during embryonic development.

Ventricular septal defect type 1 (VSD1) is a type of congenital heart defect where there is a hole in the wall that separates the lower chambers (ventricles) of the heart. This hole allows oxygen-rich blood from the left ventricle to mix with oxygen-poor blood from the right ventricle.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the sequencing of multiple genes or even the entire genome at once. It can be used to identify genetic mutations or variants that may be associated with certain diseases or conditions.

Therefore, a “GATA4 Gene Ventricular septal defect type 1 NGS Genetic Test” would involve sequencing the GATA4 gene using NGS technology to identify any genetic mutations or variants that may be associated with ventricular septal defect type 1. This test can help in diagnosing the condition, understanding its genetic basis, and potentially identifying individuals who may be at risk of developing the condition.