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KCNJ2 Gene Short QT syndrome type 3 NGS Genetic DNA Test Cost 20000 Rs
KCNJ2 Gene Short QT syndrome type 3 NGS Genetic DNA Test Details
KCNJ2 Gene Short QT Syndrome Type 3 NGS Genetic DNA Test
Introduction
Short QT Syndrome (SQTS) is a rare genetic disorder that affects the electrical activity of the heart. KCNJ2 is one of the genes associated with Short QT Syndrome type 3 (SQTS3). The KCNJ2 gene is responsible for encoding the inward rectifier potassium channel (Kir2.1), which plays a crucial role in regulating the heart's electrical activity. In this blog, we will discuss the symptoms, diagnosis, and cost of the KCNJ2 gene Short QT Syndrome type 3 NGS genetic DNA test offered by DNA Labs India.
Symptoms of Short QT Syndrome Type 3
The symptoms of Short QT Syndrome type 3 can vary from person to person, and some individuals may not have any symptoms at all. However, the following symptoms are commonly observed in individuals with SQTS3:
- Fainting or syncope
- Palpitations or rapid heartbeat
- Chest pain
- Sudden cardiac arrest or sudden death
Diagnosis of Short QT Syndrome Type 3
The diagnosis of Short QT Syndrome type 3 involves a thorough evaluation of the patient's medical history, physical examination, and various tests, including:
- Electrocardiogram (ECG) - This test records the electrical activity of the heart and can detect any abnormalities in the heart rhythm.
- Echocardiogram - This test uses ultrasound waves to create an image of the heart and can identify any structural abnormalities.
- Cardiac magnetic resonance imaging (MRI) - This test uses magnetic fields and radio waves to create detailed images of the heart and can detect any structural abnormalities.
- Genetic testing - This test involves analyzing the patient's DNA for mutations in the KCNJ2 gene and other genes associated with Short QT Syndrome.
KCNJ2 Gene Short QT Syndrome Type 3 NGS Genetic DNA Test
The KCNJ2 gene Short QT Syndrome type 3 NGS genetic DNA test offered by DNA Labs India is a cutting-edge genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the patient's DNA for mutations in the KCNJ2 gene. This test can accurately identify mutations in the KCNJ2 gene that are associated with Short QT Syndrome type 3.
The test involves collecting a small sample of the patient's blood or saliva, which is then sent to the DNA Labs India laboratory for analysis. The test typically takes 2-3 weeks to complete, after which the patient and their healthcare provider will receive a detailed report of the test results.
Cost of KCNJ2 Gene Short QT Syndrome Type 3 NGS Genetic DNA Test
The cost of the KCNJ2 gene Short QT Syndrome type 3 NGS genetic DNA test offered by DNA Labs India is INR 20,000. This cost includes the genetic testing, analysis, and a detailed report of the test results.
Conclusion
Short QT Syndrome type 3 is a rare genetic disorder that can have serious consequences if left untreated. The KCNJ2 gene Short QT Syndrome type 3 NGS genetic DNA test offered by DNA Labs India is a highly accurate and reliable test that can help diagnose this condition and guide appropriate treatment. If you or someone you know is experiencing symptoms of Short QT Syndrome, it is important to speak with a healthcare professional and consider genetic testing to determine the underlying cause of the condition.
Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for KCNJ2 Gene Short QT syndrome type 3 NGS Genetic DNA Test