Cardiomyopathy is a condition that affects the heart muscle, making it harder for the heart to pump blood to the rest of the body. One specific form of this condition is Dilated Cardiomyopathy (DCM), which is characterized by the dilation and weakening of the heart’s ventricles. Genetic factors play a significant role in the development […]
— The ACTN2 gene plays a critical role in the structure and function of heart muscle cells. Mutations in this gene can lead to a condition known as cardiomyopathy, specifically dilated cardiomyopathy type 1AA. This genetic disorder affects the heart’s ability to pump blood efficiently, leading to a range of symptoms that can significantly impact […]
Cardiomyopathy is a group of diseases that affect the heart muscle. Among these, Dilated Cardiomyopathy (DCM) is a condition characterized by the dilation of the ventricles, which impairs the heart’s ability to pump blood efficiently. Genetic factors play a significant role in the development of DCM, with the DSG2 gene being one of the critical […]
— Cardiac defects are among the most common birth defects, affecting millions of people worldwide. Advances in genetics have paved the way for identifying the genetic underpinnings of many of these conditions. One such gene, CNOT3, has been linked to cardiac defects, highlighting the importance of genetic testing for individuals at risk. DNA Labs UAE […]
DNA Labs UAE is at the forefront of genetic testing and research, providing a comprehensive suite of services aimed at understanding and diagnosing genetic conditions. Among its array of tests, the PPP1R8 Gene Cardiac Defects PPP1R8 Related Genetic Test stands out for its critical role in diagnosing cardiac defects associated with the PPP1R8 gene. This […]
Understanding the nuances of genetic conditions is crucial for early diagnosis and management. Among these conditions, the GATA6 gene mutation leading to Atrial Septal Defect Type 9 (ASD9) is significant. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive services to detect such conditions. This article delves into the symptoms associated with […]
The FLNA gene plays a crucial role in the human body, coding for the protein filamin A, which is involved in cell structure, movement, and signaling. Mutations in the FLNA gene can lead to a variety of conditions, one of which is Cardiac Valvular Dysplasia, an X-linked genetic disorder. This condition primarily affects the heart’s […]
Understanding the intricacies of genetic conditions is essential for early diagnosis and effective treatment. Among these, the GATA4 gene mutation stands out due to its significant role in causing Atrioventricular Septal Defect Type 4 (AVSD4). This condition is a congenital heart defect characterized by a combination of heart problems affecting the atria and ventricles. DNA […]
Cardioencephalomyopathy due to cytochrome c oxidase deficiency, particularly related to mutations in the SCO2 gene, is a rare and often fatal condition that affects infants. This genetic disorder disrupts the normal functioning of mitochondria, the powerhouses of cells, leading to severe symptoms in affected individuals. Understanding the symptoms and the importance of early genetic testing […]
Understanding the intricacies of genetic conditions is crucial for early diagnosis and effective management. Among these conditions, the Atrioventricular Septal Defect (AVSD) stands out due to its impact on the heart’s structure and function. Specifically, mutations in the GATA6 gene have been linked to AVSD Type 5, a condition that necessitates prompt and accurate diagnosis […]
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.
