Understanding SLCO1B3 Gene Hyperbilirubinemia Rotor Type Hyperbilirubinemia Rotor type is a rare genetic disorder that affects the liver’s ability to process bilirubin, a yellow compound that occurs in the blood as a byproduct of the breakdown of red blood cells. This condition leads to an increase in bilirubin levels in the bloodstream, causing the skin […]
Symptoms of PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 with or Without Anosmia Genetic Test Hypogonadotropic hypogonadism (HH) type 3 is a condition characterized by a lack of sexual development associated with deficient production or action of gonadotropin-releasing hormone (GnRH), which is essential for the stimulation of sex hormone production in the body. This condition can […]
Hyperparathyroidism Type 1, also known as familial isolated hyperparathyroidism, is a condition characterized by the overactivity of the parathyroid glands. This overactivity results in the excessive production of parathyroid hormone (PTH), leading to abnormal calcium levels in the blood. The condition is often linked to mutations in the CDC73 gene, which plays a crucial role […]
Symptoms of GNRHR Gene Hypogonadotropic Hypogonadism Type 7 with or Without Anosmia Genetic Test Hypogonadotropic hypogonadism (HH) type 7 is a rare genetic condition that affects the normal development of the reproductive system. This condition, caused by mutations in the GNRHR gene, can occur with or without anosmia (the loss of the sense of smell). […]
Hyperparathyroidism Type 2 is a rare genetic condition that affects the parathyroid glands, leading to an overproduction of parathyroid hormone (PTH). This overproduction can cause a range of symptoms and complications, including weakened bones, kidney stones, and neurological issues. The condition is often familial, meaning it is passed down through families. A significant breakthrough in […]
Symptoms of CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test Hemolytic Uremic Syndrome (HUS) is a serious condition that affects the blood and blood vessels, leading to the destruction of blood platelets (cells involved in clotting), a low red blood cell count (anemia), and kidney failure due to damage to the very small blood vessels of […]
At DNA Labs UAE, we are committed to providing advanced genetic testing services to help individuals understand their health better and take proactive steps towards managing it. One of the specialized tests we offer is the CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test, a crucial screening for individuals who may be at risk of developing […]
Hemolytic Uremic Syndrome (HUS) is a serious condition characterized by the triad of hemolytic anemia, acute kidney failure (uremia), and a low platelet count (thrombocytopenia). It predominantly affects children but can occur at any age. Among the genetic forms of HUS, mutations in the CFHR3 (Complement Factor H Related Protein 3) gene have been identified […]
Understanding CFHR4 Gene Hemolytic Uremic Syndrome Hemolytic Uremic Syndrome (HUS) is a rare but serious condition characterized by the triad of hemolytic anemia, acute kidney failure (uremia), and a low platelet count (thrombocytopenia). Among the genetic factors contributing to this condition, mutations in the CFHR4 gene have been identified as a potential cause. Recognizing the […]
Certainly! Here’s a detailed article on the symptoms of CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test, including the test cost and a backlink URL to DNA Labs UAE. Symptoms of CFHR5 Gene Hemolytic Uremic Syndrome Hemolytic Uremic Syndrome (HUS) is a rare but serious condition that affects the blood and blood vessels. It results in […]
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.
