In the realm of genetic diagnostics, the identification and understanding of specific gene mutations have opened new avenues for the treatment and management of various diseases. One such condition that has garnered attention is CD59 Gene Hemolytic Anemia, which can present with or without immune-mediated polyneuropathy. This condition is rooted in genetic anomalies that affect […]
Hematology Diseases
Symptoms and Testing information for C15orf41 Gene Dyserythropoietic Anemia Congenital Type 1B Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide array of services aimed at understanding genetic conditions and providing actionable insights for patients and healthcare providers. One such condition that has garnered attention is Dyserythropoietic Anemia Congenital Type 1B, which is linked to mutations in the C15orf41 gene. This […]
Symptoms and Testing information for KEL Gene Hemolytic Anemia Kell-System Related Genetic Test
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 […]
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 TSR2 Gene Diamond-Blackfan Anemia Type 14 with Mandibulofacial Dysostosis Genetic Test
Understanding Diamond-Blackfan Anemia Type 14 with Mandibulofacial Dysostosis Diamond-Blackfan Anemia (DBA) is a rare genetic disorder characterized by the failure of the bone marrow to produce adequate red blood cells. This condition can lead to severe anemia and various physical abnormalities. A particular subtype of this condition, known as Diamond-Blackfan Anemia Type 14 with Mandibulofacial […]