Duchenne Muscular Dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Cardiomyopathy, particularly dilated cardiomyopathy, is a common complication associated with DMD, known as DMD gene cardiomyopathy dilated type 3B. This condition specifically affects the […]
Pneumology Diseases
Symptoms and Testing information for CSRP3 Gene Cardiomyopathy dilated type 1M Genetic Test
Symptoms of CSRP3 Gene Cardiomyopathy Dilated Type 1M Genetic Test 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 disease, dilated cardiomyopathy (DCM), can be caused by genetic mutations, including those in the CSRP3 gene. […]
Symptoms and Testing information for TCAP Gene Cardiomyopathy dilated type 1N Genetic Test
Symptoms of TCAP Gene Cardiomyopathy Dilated Type 1N Genetic Test Cardiomyopathy is a group of diseases that affect the heart muscle, making it harder for the heart to pump blood to the rest of the body. Among the different types, Dilated Cardiomyopathy (DCM) is a prevalent form, characterized by the dilation and weakening of the […]
Symptoms and Testing information for LDB3 Gene Cardiomyopathy Dilated Type 1C Genetic Test
Cardiomyopathy is a term that refers to diseases of the heart muscle. Among these, dilated cardiomyopathy (DCM) is a condition that primarily affects the heart’s ventricles and atria, which are the lower and upper chambers of the heart, respectively. The condition is characterized by the dilation and impaired contraction of the ventricles, which can lead […]
Symptoms and Testing information for NEXN Gene Cardiomyopathy Dilated Type 1CC Genetic Test
In the realm of genetic testing and diagnostics, understanding the nuances of specific genetic conditions is paramount for both patients and healthcare providers. One such condition that has garnered attention in recent years is the NEXN gene-related cardiomyopathy, specifically the dilated type 1CC. DNA Labs UAE stands at the forefront of genetic testing services, offering […]
Symptoms and Testing information for TNNT2 Gene Cardiomyopathy Dilated Type 1D Genetic Test
Understanding the genetic underpinnings of various diseases is crucial for early detection, accurate diagnosis, and effective management. Among the conditions that have seen significant advancements in genetic testing is Cardiomyopathy, specifically Dilated Cardiomyopathy (DCM) linked to the TNNT2 gene. This article delves into the symptoms of TNNT2 Gene Cardiomyopathy Dilated Type 1D, the importance of […]
Symptoms and Testing information for RBM20 Gene Cardiomyopathy Dilated Type 1DD Genetic Test
Cardiomyopathy is a disease that affects the heart muscle, making it harder for the heart to pump blood to the rest of the body. Dilated cardiomyopathy (DCM) is a common form, characterized by an enlarged and weakened heart. Among the genetic factors contributing to DCM, mutations in the RBM20 gene have been identified as a […]
Symptoms and Testing information for SCN5A Gene Cardiomyopathy Dilated Type 1E Genetic Test
Symptoms of SCN5A Gene Cardiomyopathy Dilated Type 1E Genetic Test Cardiomyopathy is a condition that affects the muscle of the heart, impairing its ability to pump blood effectively throughout the body. Dilated cardiomyopathy (DCM) is one of the most common types, characterized by the dilation and weakening of the heart’s main pumping chamber. Among the […]
Symptoms and Testing information for MYH6 Gene Cardiomyopathy Dilated Type 1EE Genetic Test
Symptoms of MYH6 Gene Cardiomyopathy Dilated Type 1EE Genetic Test Cardiomyopathy is a disease that affects the muscle tissue of the heart, making it harder for the heart to pump blood to the rest of the body. One specific form, Dilated Cardiomyopathy (DCM), involves the enlargement of the heart’s chambers and thinning of its walls, […]
Symptoms and Testing information for BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test
Symptoms of BRAF Gene Cardiofaciocutaneous Syndrome Genetic Test Cardiofaciocutaneous (CFC) syndrome is a rare genetic condition that affects various parts of the body, including the heart, facial features, and skin. This condition is primarily caused by mutations in several genes, including the BRAF gene. Recognizing the symptoms of CFC syndrome is crucial for early diagnosis […]