Symptoms of SNTA1 Gene Long QT Syndrome Type 12 Long QT Syndrome Type 12, associated with mutations in the SNTA1 gene, is a rare inherited condition that can lead to serious heart rhythm abnormalities. It is crucial for individuals to be aware of the symptoms associated with this condition to seek timely medical intervention. The […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide individuals with vital health information. Among its extensive portfolio of genetic tests, the KCNJ5 Gene Long QT Syndrome Type 13 Genetic Test stands out as a critical tool for diagnosing this rare but serious […]
Symptoms of CALM2 Gene Long QT Syndrome Type 15 Long QT Syndrome (LQTS) is a disorder of the heart’s electrical activity. It can cause sudden, uncontrollable, and dangerous arrhythmias in response to exercise or stress. Type 15, specifically linked to mutations in the CALM2 gene, is a rare but significant variant of this condition. Recognizing […]
Understanding DSP Gene Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis Dilated Cardiomyopathy (DCM) is a condition characterized by the dilation of the heart’s ventricles and impaired systolic function, leading to heart failure and arrhythmias. When associated with mutations in the Desmoplakin (DSP) gene, this condition can manifest alongside distinctive physical traits, such as […]
DNA Labs UAE is at the forefront of genetic testing, providing a wide range of services designed to offer insights into various genetic conditions. Among these tests, the MYLK2 Gene Cardiomyopathy Hypertrophic Midventricular Digenic Genetic Test is a critical tool for diagnosing a specific form of cardiomyopathy. This article explores the symptoms associated with this […]
Understanding DBH Gene Dopamine beta-hydroxylase (DBH) Deficiency Dopamine beta-hydroxylase (DBH) deficiency is a rare genetic disorder that affects the autonomic nervous system by disrupting the production of the enzyme dopamine beta-hydroxylase. This enzyme is crucial for the synthesis of norepinephrine from dopamine, a key step in the catecholamine pathway that is essential for the proper […]
Symptoms of MT-TG Gene Cardiomyopathy Hypertrophic MT-TG Related Genetic Test Cardiomyopathy is a condition that affects the muscle of the heart, causing it to become enlarged, thick, or rigid. Among the various types of cardiomyopathy, hypertrophic cardiomyopathy (HCM) is notable for the thickening of the heart muscle, which can lead to health complications such as […]
Symptoms of SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test Familial Atrial Fibrillation (FAF) is a type of heart disorder characterized by an irregular and often rapid heart rate that can increase the risk of strokes, heart failure, and other heart-related complications. Among the genetic factors contributing to this condition, mutations in the SCN1B […]
Understanding the Symptoms of PLN Gene Cardiomyopathy Hypertrophic Type 18 and the Importance of Genetic Testing Cardiomyopathy is a disease of the heart muscle that makes it harder for the heart to pump blood to the rest of the body. One specific type, known as Hypertrophic Cardiomyopathy (HCM), is particularly noteworthy because it often goes […]
Understanding the nuances of genetic conditions is crucial in providing targeted and effective healthcare. Among the myriad of genetic conditions that have a profound impact on the human body, heart-related genetic conditions hold a significant place due to their critical nature. One such condition is the heart block progressive familial type 1A, which is linked […]
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.
