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Symptoms and Testing information for ALDH1A2 Gene Tetralogy of Fallot Genetic Test

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 and Testing information for GATA4 Gene Tetralogy of Fallot Genetic Test

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

Symptoms and Testing information for GATA6 Gene Tetralogy of Fallot Genetic Test

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

Symptoms and Testing information for ZFPM2 Gene Tetralogy of Fallot Genetic Test

— 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

Symptoms and Testing information for MED13L Gene Transposition of the Great Arteries Dextro-Looped 1 Genetic Test

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 and Testing information for GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test

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

Symptoms and Testing information for CITED2 Gene Ventricular Septal Defect Type 2 Genetic Test

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

Symptoms and Testing information for MT-TE Gene Mitochondrial myopathy infantile transient MT-TE related Genetic Test

Mitochondrial myopathies are a group of neuromuscular diseases caused by damage to the mitochondria, the tiny energy factories found inside almost every cell in our body. These conditions can lead to a wide range of health problems, affecting various systems within the body. One specific form of this disease is the infantile transient mitochondrial myopathy

Symptoms and Testing information for CRHR1 Gene Pulmonary newborn hypertension Genetic Test

Pulmonary hypertension in newborns, also known as neonatal pulmonary hypertension, is a serious and potentially life-threatening condition characterized by high blood pressure in the lungs’ arteries. This condition can significantly impact the oxygenation of the newborn’s body, leading to critical health issues. Recent advancements in genetic research have identified a connection between the CRHR1 gene

Symptoms and Testing information for MT-ATP8 Gene Cardiomyopathy infantile hypertrophic MT-ATP8 related Genetic Test

Symptoms of MT-ATP8 Gene Cardiomyopathy Infantile Hypertrophic MT-ATP8 Related Genetic Test Cardiomyopathy is a condition that affects the muscle of the heart, hindering its ability to pump blood effectively to the rest of the body. Among its various types, the infantile hypertrophic cardiomyopathy related to the MT-ATP8 gene mutation is particularly severe due to its