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 […]
In the realm of genetic testing and diagnosis, advancements have been pivotal in identifying and managing congenital heart defects, one of which is the Tetralogy of Fallot (TOF). At the forefront of these advancements is the ALDH1A2 gene Tetralogy of Fallot genetic test, a specialized diagnostic tool designed to detect mutations associated with TOF. DNA […]
Symptoms of GATA4 Gene Tetralogy of Fallot Genetic Test Tetralogy of Fallot (ToF) is a congenital heart defect that is complex and multifactorial in nature. It is characterized by four heart defects that occur together: a ventricular septal defect (VSD), pulmonary stenosis, right ventricular hypertrophy, and an overriding aorta. While the exact cause of ToF […]
In the realm of genetic testing and diagnostics, the advancement of technology has paved the way for identifying and understanding complex congenital heart defects such as Tetralogy of Fallot (TOF). Among the significant breakthroughs is the identification of the GATA6 gene’s role in the development of TOF. DNA Labs UAE stands at the forefront of […]
— Understanding the critical role genetics play in various heart conditions has been a game-changer in medical science. Among these, Tetralogy of Fallot (TOF) stands out as a congenital heart defect characterized by four specific heart problems present at birth. This condition, which alters the normal flow of blood through the heart, can have life-altering […]
The SMAD2 gene plays a crucial role in the development and maintenance of body tissues, including the cardiovascular system. Mutations in this gene can lead to serious conditions, one of which is thoracic aortic aneurysm dissection (TAAD). This condition is characterized by the weakening and subsequent tearing of the aorta’s wall, which can lead to […]
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 […]
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.
