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 […]
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 of RASA1 Gene Parkes Weber Syndrome Genetic Test Parkes Weber Syndrome is a rare congenital condition characterized by a combination of arteriovenous malformations (AVMs) and capillary malformation-arteriovenous malformations (CM-AVMs). These vascular anomalies can lead to a range of symptoms, varying in severity among individuals. The RASA1 gene plays a crucial role in the development […]
Understanding SERPINE1 Gene and Its Importance The SERPINE1 gene is responsible for the production of plasminogen activator inhibitor type 1 (PAI-1), a protein that plays a crucial role in the regulation of blood clotting. Variations in this gene can lead to either an increase or decrease in PAI-1 levels, affecting the body’s ability to form […]
Polyarteritis nodosa (PAN) is a rare, potentially life-threatening disease characterized by the inflammation of blood vessels (vasculitis), which can damage organs throughout the body. The childhood-onset form of this disease, associated with mutations in the ADA2 gene, presents unique challenges and symptoms that are critical to recognize for early diagnosis and treatment. DNA Labs UAE […]
### Article: Protein C deficiency is a rare genetic disorder that affects the blood’s ability to clot properly, leading to an increased risk of developing blood clots. The PROC gene is responsible for producing protein C, and mutations in this gene can lead to either Type I or Type II protein C deficiency. Understanding the […]
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 […]
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 […]
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 […]
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 […]
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.
