Symptoms of KCNE3 Gene Brugada Syndrome Type 6 Brugada Syndrome is a potentially life-threatening heart condition that can cause dangerous irregular heart rhythms. This condition, which is genetic, can lead to sudden cardiac arrest in individuals without any underlying heart disease. The KCNE3 gene has been identified as one of the genetic contributors to Brugada […]
Brugada Syndrome is a potentially life-threatening heart rhythm disorder that is sometimes inherited. It can lead to sudden cardiac arrest, making understanding and diagnosing this condition crucial. One specific form of this syndrome, Brugada Syndrome Type 7, is linked to mutations in the SCN3B gene. DNA Labs UAE offers a comprehensive genetic test for this […]
— Brugada Syndrome is a potentially life-threatening heart condition that can lead to dangerous arrhythmias. This syndrome is genetically inherited, and one of the genes associated with this condition is the HCN4 gene. The HCN4 Gene Brugada Syndrome Type 8 Genetic Test is a crucial diagnostic tool for individuals suspected of having this syndrome or […]
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a form of heart disease that affects the muscle of the right ventricle of the heart. It is a condition that can lead to heart failure and arrhythmias, which are irregular heartbeats that can be life-threatening. One of the genetic markers associated with this condition is the DSG2 gene. […]
Understanding the symptoms and genetic underpinnings of Atrial Septal Defect Type 5 (ASD5) is crucial for early diagnosis and treatment. This condition, associated with mutations in the ACTC1 gene, represents a significant concern for individuals and families affected by it. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the […]
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a complex genetic condition affecting the heart muscle, particularly the right ventricle. It’s characterized by the progressive replacement of cardiac muscle with fatty and fibrous tissue, leading to arrhythmias and heart failure. Type 11 of this condition, linked to mutations in the DSC2 gene, is a focus for those […]
Atrial Septal Defect (ASD) is a heart condition that is often diagnosed at birth or in early childhood. However, there are instances where the condition remains undetected until adulthood. Type 6 Atrial Septal Defect, linked to the TLL1 gene, is a rare but significant form of this condition. Recognizing the symptoms early on can lead […]
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a complex genetic condition that primarily affects the myocardium of the heart, leading to the replacement of cardiac muscle with fibrous or fatty tissue. This progressive disease can result in heart rhythm problems, heart failure, and even sudden cardiac death, particularly in young athletes. Type 12 of this condition, […]
Atrial Septal Defect (ASD) is a congenital heart defect characterized by a hole in the wall (septum) that divides the upper chambers (atria) of the heart. This condition allows oxygen-rich blood to mix with oxygen-poor blood, causing various symptoms and complications. Type 8 Atrial Septal Defect, linked to mutations in the CITED2 gene, represents a […]
Symptoms of TMEM43 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Genetic Test Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a type of genetic heart disease that primarily affects the myocardium of the right ventricle. Among its various types, ARVC Type 5 is notably caused by mutations in the TMEM43 gene. This condition is characterized by the […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
