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 […]
DNA Labs UAE is at the forefront of genetic testing and research, providing a comprehensive suite of services aimed at understanding and diagnosing genetic conditions. Among its array of tests, the PPP1R8 Gene Cardiac Defects PPP1R8 Related Genetic Test stands out for its critical role in diagnosing cardiac defects associated with the PPP1R8 gene. This […]
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 […]
Understanding the genetic underpinnings of atrial fibrillation (AF) can provide crucial insights into its diagnosis, management, and treatment. One such genetic marker linked to the condition is the ABCC9 gene, which has been associated with Atrial Fibrillation Type 12. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the ABCC9 […]
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.
