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 […]
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a complex genetic condition that affects the myocardium, leading to the replacement of cardiac muscle with fibrous or fatty tissue. This process primarily impacts the right ventricle, causing a range of cardiovascular symptoms and increasing the risk of sudden cardiac death, especially among young athletes. Among the genes implicated […]
Symptoms of PKP2 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 9 Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Type 9, caused by mutations in the PKP2 gene, is a form of heart disease that primarily affects the muscle of the right ventricle. This condition can lead to heart rhythm abnormalities, heart failure, and sudden cardiac death, especially in […]
Arrhythmogenic Right Ventricular Dysplasia (ARVD), specifically Type 2, associated with mutations in the RYR2 gene, is a rare genetic condition that affects the heart muscle. This condition can lead to arrhythmias, heart failure, and sudden cardiac death, especially in young athletes and seemingly healthy individuals. Understanding the symptoms and undergoing genetic testing can be crucial […]
Understanding the genetic underpinnings of atrial fibrillation (AF) can significantly improve the diagnosis and management of this condition. One of the genetic markers associated with AF is the SCN5A gene. Mutations in the SCN5A gene have been linked to Atrial Fibrillation Type 10, a subtype of AF. Recognizing the symptoms associated with this genetic form […]
Understanding the symptoms and genetic basis of atrial fibrillation is crucial for effective diagnosis and management. Atrial fibrillation type 11, linked to mutations in the GJA5 gene, is a condition that affects the heart’s rhythm, leading to various symptoms and potential complications. DNA Labs UAE offers a comprehensive genetic test for this condition, providing insights […]
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.
