Ventricular tachycardia catecholaminergic polymorphic type 4 (CPVT4) is a rare but serious genetic condition that affects the heart’s rhythm. It is characterized by an abnormal heart rhythm that can lead to fainting spells, seizures, or even sudden death, especially during physical activity or emotional stress. This condition is caused by mutations in the CALM1 gene, […]
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is a rare, genetic arrhythmogenic disorder characterized by an abnormal heart rhythm. As a type of ventricular tachycardia, CPVT can lead to severe and potentially life-threatening symptoms, especially under physical stress or emotional excitement. Among the genetic variants responsible for CPVT, mutations in the TRDN gene, leading to CPVT type […]
Wolff-Parkinson-White (WPW) Syndrome is a rare congenital heart disorder characterized by an abnormal extra electrical pathway in the heart, which leads to episodes of rapid heart rate (tachycardia). In some individuals, this condition is linked to mutations in the PRKAG2 gene. Understanding the symptoms and undergoing genetic testing for PRKAG2 gene mutations can be crucial […]
Symptoms of AGK Gene Sengers Syndrome Genetic Test Sengers Syndrome is a rare genetic condition that affects multiple systems in the body, including the heart, muscles, and eyes. It is caused by mutations in the AGK gene, which plays a crucial role in the production of energy within cells. This condition is inherited in an […]
Short QT Syndrome Type 1 (SQTS1) is a rare but serious genetic condition that affects the heart’s electrical activity, potentially leading to life-threatening arrhythmias. The KCNH2 gene, which plays a critical role in the heart’s electrical signaling, is often at the center of this condition. DNA Labs UAE offers a comprehensive genetic test for those […]
The realm of genetics has made significant strides in identifying and understanding various genetic disorders that affect the human population. One such advancement is in the field of cardiology, particularly in diagnosing and managing Short QT Syndrome (SQTS). Among the genetic tests available, the KCNQ1 Gene Short QT Syndrome Type 2 Genetic Test stands out […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that empower individuals with the knowledge they need to make informed decisions about their health. One of the specialized tests we offer is the KCNJ2 Gene Short QT Syndrome Type 3 Genetic Test. This test is critical for individuals who may be […]
Symptoms of SCN5A Gene Sick Sinus Syndrome Type 1 Genetic Test Sick Sinus Syndrome Type 1, a condition characterized by a range of cardiac abnormalities, is increasingly becoming a concern for many. This syndrome, rooted in genetic anomalies, specifically involves mutations in the SCN5A gene. Recognizing the symptoms early on can significantly aid in managing […]
Symptoms of MYH6 Gene Sick Sinus Syndrome Type 3 Genetic Test Sick Sinus Syndrome (SSS) is a collection of heart rhythm disorders primarily affecting the sinus node, the heart’s natural pacemaker. Among these, Type 3 Sick Sinus Syndrome, attributed to mutations in the MYH6 gene, presents unique challenges and symptoms. DNA Labs UAE offers a […]
In the quest to understand and manage genetic disorders effectively, DNA Labs UAE has been at the forefront of providing comprehensive genetic testing services. Among the various tests offered, the CACNA1D Gene Sinoatrial Node Dysfunction and Deafness Genetic Test stands out for its importance in diagnosing a rare but significant condition that affects both 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.
