In the realm of genetic diagnostics and personalized medicine, understanding the intricate relationships between genes and health conditions is paramount. One such gene, CALCRL, plays a crucial role in the vascular system, and deficiencies in this gene can lead to a range of symptoms and health issues. DNA Labs UAE is at the forefront of […]
Cardiovascular Diseases
Symptoms and Testing information for GNA13 Gene Vascular System Defects Due to GNA13 Deficiency Genetic Test
The vascular system plays a critical role in maintaining the homeostasis of the human body, distributing essential nutrients and oxygen to various organs while removing waste products. Genetic abnormalities can significantly impair this system’s functionality, leading to severe health implications. One such genetic concern is related to the GNA13 gene, which, when deficient, can lead […]
Symptoms and Testing information for PROS1 Gene Protein S Deficiency Autosomal Dominant Genetic Test
Symptoms of PROS1 Gene Protein S Deficiency Protein S deficiency is a rare genetic disorder that affects the blood’s ability to clot properly, leading to an increased risk of developing abnormal blood clots. This condition is associated with mutations in the PROS1 gene, which plays a crucial role in the regulation of blood clotting. Individuals […]
Symptoms and Testing information for KLHL3 Gene Pseudohypoaldosteronism Type 2D Genetic Test
Pseudohypoaldosteronism Type 2D, also known as Familial Hyperkalemia and Hypertension (FHHt), is a rare genetic disorder that disrupts the normal balance of potassium, sodium, and chloride in the body. This imbalance leads to a range of symptoms and complications. The KLHL3 gene has been identified as one of the genetic contributors to this condition. DNA […]
Symptoms and Testing information for NR3C2 Gene Hypertension Early Onset Genetic Test
In the realm of medical genetics, understanding the underlying causes of diseases has always been a cornerstone for developing effective treatments and preventive measures. One such condition that has garnered significant attention is hypertension, particularly the early-onset form that is influenced by genetic factors. Among the genes implicated in this condition, the NR3C2 gene plays […]
Symptoms and Testing information for CUL3 Gene Pseudohypoaldosteronism Type 2E Genetic Test
Pseudohypoaldosteronism Type 2E, also known as Familial Hyperkalemia and Hypertension (FHHt), is a rare genetic disorder that affects the body’s ability to properly regulate blood pressure and potassium levels. It is caused by mutations in the CUL3 gene, which plays a crucial role in the regulation of electrolyte balance and blood pressure. Recognizing the symptoms […]
Symptoms and Testing information for ADD2 Gene Hypertension ADD2 Related Genetic Test
Understanding the ADD2 Gene and Its Role in Hypertension Hypertension, commonly known as high blood pressure, is a complex condition that affects millions of people worldwide. It’s a leading risk factor for heart disease, stroke, and even kidney problems. While lifestyle factors such as diet, exercise, and stress management play a crucial role in managing […]
Symptoms and Testing information for BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test
Understanding BMPR2 Gene Pulmonary Hypertension Primary Type Genetic Test Pulmonary Hypertension (PH) is a complex and serious condition characterized by high blood pressure in the lungs’ arteries, leading to heart failure if left untreated. Among the various forms of Pulmonary Hypertension, Heritable Pulmonary Arterial Hypertension (HPAH) is a significant subtype, often caused by mutations in […]
Symptoms and Testing information for CYP3A5 Gene Hypertension Salt-Sensitive Essential Susceptibility to Genetic Test
— Hypertension, or high blood pressure, is a common but serious health condition that affects millions of people worldwide. While lifestyle factors such as diet, exercise, and stress management play crucial roles in managing hypertension, genetics also has a significant part in determining an individual’s susceptibility to this condition. Among the genetic factors implicated in […]
Symptoms and Testing information for BMPR2 Gene Pulmonary Venoocclusive Disease Type 1 Genetic Test
Pulmonary Venoocclusive Disease (PVOD) is a rare form of pulmonary hypertension that results from the obstruction of small veins in the lungs. Among the genetic causes of this condition, mutations in the BMPR2 gene are significant contributors. Understanding the symptoms of BMPR2 Gene Pulmonary Venoocclusive Disease Type 1 and the importance of genetic testing is […]