— 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 […]
Brugada Syndrome is a rare but serious condition that affects the heart’s rhythm. It is a genetic disorder that can lead to sudden cardiac arrest in seemingly healthy individuals, often during sleep. Among the several genetic variants linked to Brugada Syndrome, Type 9 is associated with mutations in the SLMAP gene. Recognizing the symptoms and […]
— Cardiac defects are among the most common birth defects, affecting millions of people worldwide. Advances in genetics have paved the way for identifying the genetic underpinnings of many of these conditions. One such gene, CNOT3, has been linked to cardiac defects, highlighting the importance of genetic testing for individuals at risk. DNA Labs UAE […]
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 […]
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.
