Short Description

NGS genetic DNA test detecets for variant and mutation detection in ALDH1A2 gene for Tetralogy of Fallot

PreTest Information

Clinical History of Patient who is going for ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test gene ALDH1A2

Detail Description

ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test

Tetralogy of Fallot is a congenital heart defect that affects the normal flow of blood through the heart. This condition is caused by a combination of four heart defects that occur during fetal development. Tetralogy of Fallot affects about 1 in every 2,500 newborns and is more common in males than females. The condition can be diagnosed in the early stages of pregnancy through ultrasound scans or after birth by a pediatrician.

The ALDH1A2 gene has been identified as a possible genetic cause of Tetralogy of Fallot. This gene plays a critical role in the development of the heart and is responsible for the production of an enzyme that helps to break down toxic substances in the body. Mutations in this gene can interfere with the normal development of the heart, leading to the development of Tetralogy of Fallot.

The ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test is a cutting-edge genetic test that can identify mutations in the ALDH1A2 gene. This test uses Next-Generation Sequencing (NGS) technology to analyze the DNA of the patient and identify any genetic mutations that may be present. The test is highly accurate and can identify even the smallest mutations in the ALDH1A2 gene.

Symptoms of Tetralogy of Fallot

The symptoms of Tetralogy of Fallot can vary depending on the severity of the condition. Some common symptoms include:

• Bluish tint to the skin, lips, and nails (cyanosis)
• Rapid breathing
• Fainting or passing out
• Poor weight gain
• Trouble feeding
• Clubbing of fingers and toes

Diagnosis of Tetralogy of Fallot

Tetralogy of Fallot can be diagnosed in the early stages of pregnancy through ultrasound scans. After birth, a pediatrician can diagnose the condition based on the symptoms and a physical examination. Further tests, such as echocardiogram, electrocardiogram, and chest X-rays may be performed to confirm the diagnosis.

ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test Cost

The ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test is available at DNA Labs India for a cost of INR 20,000. This test is highly accurate and can provide valuable information about the genetic cause of Tetralogy of Fallot. The test is non-invasive and requires only a small blood sample from the patient.

Conclusion

Tetralogy of Fallot is a serious heart condition that can be caused by genetic mutations in the ALDH1A2 gene. The ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test is a cutting-edge genetic test that can identify these mutations and provide valuable information about the condition. This test is available at DNA Labs India for a cost of INR 20,000 and is highly accurate and non-invasive. If you or someone you know is experiencing symptoms of Tetralogy of Fallot, it is important to seek medical attention as soon as possible.

Contact DNA Labs India today to learn more about the ALDH1A2 Gene Tetralogy of Fallot NGS Genetic DNA Test and how it can help in the diagnosis and treatment of this condition.