Moyamoya disease is a rare, progressive cerebrovascular disorder characterized by the narrowing of the carotid artery in the brain and the development of tiny blood vessels that form a “puff of smoke” appearance (moyamoya is Japanese for “puff of smoke”) on angiographic images. This condition can lead to strokes, transient ischemic attacks (TIAs), and cognitive […]
The LPIN1 gene plays a crucial role in the metabolism of lipids in our bodies. Mutations in this gene can lead to a rare but severe condition known as myoglobinuria acute recurrent rhabdomyolysis. This condition is characterized by episodes of muscle pain, weakness, and the release of myoglobin into the urine, potentially leading to kidney […]
DNA Labs UAE stands at the forefront of genetic testing and personalized medicine, offering a comprehensive suite of services designed to provide insights into one’s genetic blueprint. Among the myriad of tests available, the ISCU Gene Myopathy with Lactic Acidosis Hereditary Genetic Test is pivotal for individuals experiencing symptoms associated with this rare genetic disorder. […]
Understanding the nuances of our genetic makeup can be the key to unlocking a healthier, more informed lifestyle. Among the various genetic tests available, the SLC6A2 Gene Orthostatic Intolerance Genetic Test stands out for its specific focus on diagnosing a condition that affects many yet remains underdiagnosed due to its complex nature. Offered by DNA […]
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 […]
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.
