Symptoms of NPM1 and FLT3 Test Understanding the implications of genetic mutations is crucial in the realm of medical science, especially when it comes to conditions like acute myeloid leukemia (AML). Among the genetic markers that have garnered attention for their role in AML are NPM1 and FLT3. These mutations can significantly influence the prognosis […]
Genetic Diseases
Symptoms and Testing information for PDGFR Mutation Screening Exons 12 14 18 Test
DNA labs UAE offers a comprehensive PDGFR Mutation Screening Exons 12, 14, 18 Test, designed to identify mutations in the platelet-derived growth factor receptor (PDGFR) gene. These mutations can play a significant role in the development of various diseases, including certain types of cancers. Understanding the symptoms and implications of these mutations can be crucial […]
Symptoms and Testing information for PDL1 SP263 Clone Test
Understanding the Symptoms of PDL1 SP263 Clone Test Introduction The PDL1 SP263 clone test is a significant advancement in the field of medical diagnostics, particularly in the area of cancer research and treatment. This test is designed to evaluate the expression of the Programmed Death-Ligand 1 (PDL1) protein in various types of cancer cells. The […]
Symptoms and Testing information for PNH Comprehensive Work-Up Flowcytometry-Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test
Symptoms of Paroxysmal Nocturnal Hemoglobinuria (PNH) Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare, acquired, life-threatening disease of the blood characterized by the destruction of red blood cells, bone marrow failure, and blood clots. Understanding the symptoms of PNH is crucial for timely diagnosis and management of the condition. The most common symptoms include fatigue, difficulty […]
Symptoms and Testing information for Pre-implantation Genetic Screening PGS per Embryo Test
In the realm of reproductive medicine, Pre-implantation Genetic Screening (PGS) stands out as a revolutionary advancement, offering couples the hope of a healthy offspring by detecting genetic anomalies at the very earliest stage of life. At DNA Labs UAE, we are at the forefront of providing this cutting-edge technology to our clients, ensuring they are […]
Symptoms and Testing information for 1p and 19q Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide insights into your genetic makeup and how it may impact your health. Among the various tests offered, the 1p and 19q test stands out for its crucial role in diagnosing certain types of brain […]
Symptoms and Testing information for Biopsy Electron Microscopy Test
In the ever-evolving field of medical diagnostics, the Biopsy Electron Microscopy Test stands out as a pivotal procedure for the identification and analysis of various diseases at a cellular level. DNA Labs UAE, a leading genetic laboratory, offers this cutting-edge test, providing invaluable insights into the cellular structures and anomalies that traditional microscopy methods might […]
Symptoms and Testing information for Chronic Neutrophilic Leukemia CNLCSF3R Gene – Exon 14 and 17; SETBP Gene – Exon 4 Test
Chronic Neutrophilic Leukemia (CNL) is a rare myeloproliferative disorder characterized by an increase in predominantly mature neutrophils in the blood. The diagnosis and understanding of CNL have evolved significantly with the advent of genetic testing, specifically targeting mutations in the CSF3R gene (exons 14 and 17) and the SETBP1 gene (exon 4). These genetic markers […]
Symptoms and Testing information for cKIT Mutation Screening Exons 9 11 13 17 Gastrointestinal Stromal Tumors Test
Gastrointestinal Stromal Tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract, originating from the interstitial cells of Cajal or their precursors. These tumors are characterized by specific genetic mutations, with the cKIT gene mutation being one of the most prevalent. Understanding the symptoms and genetic underpinnings of GISTs is crucial for early […]
Symptoms and Testing information for Hemochromatosis Common Mutation Analysis in HFE Gene H63D S61C and C282Y Test
Hemochromatosis is a genetic disorder characterized by excessive absorption of iron by the body. This condition can lead to serious health problems, including liver disease, heart problems, and diabetes, if not diagnosed and treated early. The HFE gene plays a crucial role in regulating iron absorption, and mutations in this gene are the most common […]