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 […]
The MED13L gene plays a critical role in heart development and its mutations can lead to various congenital heart defects, including Transposition of the Great Arteries Dextro-Looped 1 (d-TGA). This condition is characterized by a reversal of the main arteries—the pulmonary artery and the aorta—resulting in oxygen-poor blood being circulated to the body and oxygen-rich […]
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 […]
In the realm of medical genetics, understanding the intricate details of our genetic makeup can be the key to unlocking personalized healthcare solutions. One such area of focus is the SCN5A gene, which has been closely linked to Ventricular Fibrillation Paroxysmal Familial Type 1 (VF PF1), a rare but potentially life-threatening condition. DNA Labs UAE […]
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 […]
Understanding GATA4 Gene Ventricular Septal Defect Type 1 Ventricular Septal Defect (VSD) Type 1 is a congenital heart defect characterized by one or more holes in the wall that separates the right and left ventricles of the heart. The GATA4 gene plays a crucial role in the development of the heart, and mutations in this […]
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 […]
Ventricular Septal Defect (VSD) Type 2 is a congenital heart defect characterized by one or more holes in the wall that separates the right and left ventricles of the heart. The CITED2 gene plays a crucial role in the development of the heart, and mutations in this gene are linked to the occurrence of VSD […]
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.
