Thrombocytopenia, particularly the Congenital Amegakaryocytic Thrombocytopenia (CAMT), is a rare but severe condition that affects the blood’s ability to clot properly due to an extremely reduced number of platelets. This disorder is directly linked to mutations in the MPL gene, which plays a crucial role in platelet formation. Recognizing the symptoms early on and undergoing […]
Symptoms of SLC19A2 Gene Thiamine-Responsive Megaloblastic Anemia Syndrome Genetic Test Thiamine-Responsive Megaloblastic Anemia Syndrome (TRMA), also known as Rogers Syndrome, is a rare autosomal recessive disorder caused by mutations in the SLC19A2 gene. This gene plays a crucial role in thiamine (vitamin B1) transport into cells, an essential process for cellular energy production and DNA […]
Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin, the protein in red blood cells that carries oxygen, is made of two different parts: alpha globin and beta globin. The HBD gene is responsible for the production of delta globin, which is […]
Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin allows red blood cells to carry oxygen from your lungs to all parts of your body, and signs of thalassemia are linked to the lack of oxygen. Among the types of thalassemia, Alpha […]
Understanding Thalassemia Alpha and the Role of the HBA1 Gene Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin allows red blood cells to carry oxygen from your lungs to all parts of your body, and a deficiency can lead to anemia. […]
Stormorken Syndrome is a rare genetic disorder that affects multiple systems within the body, leading to a variety of symptoms. It is caused by mutations in the STIM1 gene, which plays a critical role in calcium signaling within cells. This signaling is crucial for the proper functioning of muscle cells, blood cells, and other types […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive and reliable genetic testing services. One of the specialized tests we offer is for the diagnosis of Spherocytosis Type 5, which is caused by mutations in the EPB42 gene. This condition is a rare form of hereditary spherocytosis, a disorder that affects […]
Spherocytosis is a form of anemia characterized by the presence of spherocytes, or spherical red blood cells, in the bloodstream. This condition is caused by a variety of genetic mutations that affect the proteins responsible for maintaining the red blood cells’ shape and flexibility. Among these genetic mutations, the SPTA1 gene plays a crucial role, […]
Spherocytosis Type 2, caused by mutations in the SPTB gene, is a genetic condition characterized by the presence of spherocytes (sphere-shaped red blood cells) in the blood, leading to various symptoms and complications. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a comprehensive genetic test for this condition. Understanding the symptoms […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals understand their genetic makeup and manage their health better. One of the specialized tests we offer is the ANK1 Gene Spherocytosis Type 1 Genetic Test. This test is crucial for diagnosing Hereditary Spherocytosis (HS), a condition that affects the […]
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.
