Symptoms of TTN Gene Cardiomyopathy Dilated Type 1G TTN gene cardiomyopathy, also known as dilated cardiomyopathy type 1G, is a genetic disorder that affects the heart muscle, leading to its enlargement and impaired ability to pump blood efficiently. This condition is caused by mutations in the TTN gene, which plays a crucial role in the […]
Cardiofaciocutaneous (CFC) syndrome is a rare genetic condition that affects various parts of the body, including the heart (cardio-), face (facio-), and skin (cutaneous). It is caused by mutations in several genes, including the KRAS gene. Understanding the symptoms of this syndrome is crucial for early diagnosis and treatment. DNA Labs UAE offers a comprehensive […]
Understanding the symptoms of SDHA Gene Cardiomyopathy Dilated Type 1GG and the significance of genetic testing is essential for those potentially affected by this condition. DNA Labs UAE offers a comprehensive genetic test designed to identify mutations in the SDHA gene, which can lead to Dilated Cardiomyopathy (DCM) of the 1GG type. This article aims […]
Brugada Syndrome is a potentially life-threatening heart rhythm disorder that is sometimes inherited. It can lead to sudden cardiac arrest, often in young and otherwise healthy individuals. A specific genetic variation associated with this condition is found in the GPD1L gene, leading to what is known as Brugada Syndrome Type 2. DNA Labs UAE offers […]
Symptoms of CACNA1C Gene Brugada Syndrome Type 3 Brugada Syndrome is a rare but serious condition that affects the heart’s rhythm. It is a genetic disorder, meaning it is passed down through families. One of the genes associated with this condition is the CACNA1C gene, which, when mutated, can lead to Brugada Syndrome Type 3. […]
Understanding Brugada Syndrome Type 4 Brugada Syndrome is a rare but serious condition that affects the heart’s rhythm. It can lead to sudden cardiac arrest in otherwise healthy individuals, often without warning. Among the several genetic variations that can lead to Brugada Syndrome, mutations in the CACNB2 gene are responsible for what is known as […]
In the realm of genetic diagnostics and personalized medicine, understanding the intricacies of specific genetic conditions is paramount for both patients and healthcare providers. Among these conditions, Brugada Syndrome Type 5, linked to mutations in the SCN1B gene, stands out due to its significant implications for cardiac health. DNA Labs UAE is at the forefront […]
Symptoms of KCNE3 Gene Brugada Syndrome Type 6 Brugada Syndrome is a potentially life-threatening heart condition that can cause dangerous irregular heart rhythms. This condition, which is genetic, can lead to sudden cardiac arrest in individuals without any underlying heart disease. The KCNE3 gene has been identified as one of the genetic contributors to Brugada […]
Brugada Syndrome is a potentially life-threatening heart rhythm disorder that is sometimes inherited. It can lead to sudden cardiac arrest, making understanding and diagnosing this condition crucial. One specific form of this syndrome, Brugada Syndrome Type 7, is linked to mutations in the SCN3B gene. DNA Labs UAE offers a comprehensive genetic test for this […]
— Brugada Syndrome is a potentially life-threatening heart condition that can lead to dangerous arrhythmias. This syndrome is genetically inherited, and one of the genes associated with this condition is the HCN4 gene. The HCN4 Gene Brugada Syndrome Type 8 Genetic Test is a crucial diagnostic tool for individuals suspected of having this syndrome or […]
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.
