Hemolytic anemia, particularly that associated with the Kell blood group system, is a condition that can lead to serious health complications if not diagnosed and managed properly. DNA Labs UAE offers a comprehensive genetic test specifically designed to detect mutations in the KEL gene, which plays a pivotal role in this type of anemia. This […]
Hematology Diseases
Symptoms and Testing information for KIF23 Gene Dyserythropoietic Anemia Congenital Type 3 Genetic Test
At DNA Labs UAE, we are committed to providing our clients with comprehensive genetic testing services to help diagnose and manage various genetic conditions. One such condition that has been the focus of recent research and development is Dyserythropoietic Anemia Congenital Type 3, which is associated with mutations in the KIF23 gene. Understanding the symptoms […]
Symptoms and Testing information for KLF1 Gene Dyserythropoietic Anemia Congenital Type 4 Genetic Test
DNA Labs UAE is at the forefront of genetic diagnostics, offering a comprehensive suite of tests designed to pinpoint a wide range of genetic disorders. Among these, the KLF1 Gene Dyserythropoietic Anemia Congenital Type 4 Genetic Test stands out for its specificity in diagnosing a rare but significant blood disorder. This article delves into the […]
Symptoms and Testing information for F2 Gene Dysprothrombinemia Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, providing a comprehensive suite of tests designed to identify various genetic disorders, including the F2 Gene Dysprothrombinemia Genetic Test. This particular test is crucial for individuals who may be at risk of dysprothrombinemia, a rare genetic disorder that affects the blood’s ability to […]
Symptoms and Testing information for EPOR Gene Erythrocytosis Familial Type 1 Genetic Test
Erythrocytosis Familial Type 1 is a rare genetic condition characterized by an increased red blood cell mass, leading to an elevated hematocrit level. This condition is caused by mutations in the EPOR gene, which plays a crucial role in the production of red blood cells. Understanding the symptoms and undergoing genetic testing for this condition […]
Symptoms and Testing information for EGLN1 Gene Erythrocytosis Familial Type 3 Genetic Test
Erythrocytosis, a condition characterized by an abnormal increase in the number of red blood cells in the bloodstream, can lead to various health complications, including increased blood viscosity and the risk of thrombosis. Familial erythrocytosis type 3, linked to mutations in the EGLN1 gene, is a rare genetic form of this condition. DNA Labs UAE […]
Symptoms and Testing information for EPAS1 Gene Erythrocytosis Familial Type 4 Genetic Test
Erythrocytosis, or an abnormal increase in the number of red blood cells, can be caused by various factors, including genetic mutations. One such genetic condition is Familial Erythrocytosis Type 4, linked to mutations in the EPAS1 gene. Understanding the symptoms and genetic basis of this condition is crucial for accurate diagnosis and management. DNA Labs […]
Symptoms and Testing information for F10 Gene Factor X Deficiency Genetic Test
In the realm of genetic testing and diagnostics, understanding the intricacies of various genetic disorders is crucial for effective treatment and management. Among these, Factor X deficiency, a rare genetic condition that affects the blood’s ability to clot, stands out due to its potential to cause serious bleeding problems. At DNA Labs UAE, we offer […]
Symptoms and Testing information for G6PD Gene Favism Susceptibility to Genetic Test
G6PD deficiency, a genetic disorder affecting the red blood cells, is more common than many might think. This condition can lead to a wide range of health issues, from mild to severe. Understanding the symptoms and the availability of genetic testing is crucial for managing and preventing the complications associated with G6PD deficiency. DNA Labs […]
Symptoms and Testing information for CYBA Gene Granulomatous Disease Chronic Autosomal Recessive Cytochrome B-Negative Genetic Test
Granulomatous Disease, specifically the Chronic Granulomatous Disease (CGD) caused by mutations in the CYBA gene, is a rare and severe genetic disorder. This condition affects the immune system, leading to a heightened susceptibility to infections. Individuals with this disorder have immune cells (phagocytes) that cannot effectively produce reactive oxygen species due to a deficiency in […]