Symptoms and Testing information for PNH Comprehensive Work-Up Flowcytometry-Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test

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

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

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 LPL Expert Panel 1 Test

Symptoms and Testing information for LPL Expert Panel 1 Test

— Understanding the symptoms that necessitate the LPL Expert Panel 1 Test is crucial for early detection and management of related conditions. Lipoprotein Lipase (LPL) deficiency or dysfunction can lead to various metabolic and cardiovascular diseases. The LPL Expert Panel 1 Test, offered by DNA Labs UAE for 3160 AED, is designed to diagnose issues […]

Symptoms and Testing information for MDS Panel Cytogenetics and FISH del5q del7q del20q Test

Symptoms and Testing information for MDS Panel Cytogenetics and FISH del5q del7q del20q Test

Myelodysplastic Syndromes (MDS) are a group of disorders caused by poorly formed or dysfunctional blood cells. Due to the complex nature of these syndromes, accurate diagnosis and monitoring are crucial for effective management and treatment planning. One of the advanced diagnostic tools available is the MDS Panel Cytogenetics and FISH (Fluorescence In Situ Hybridization) del5q […]

Symptoms and Testing information for Metal Screen 3 Urine Test

Symptoms and Testing information for Metal Screen 3 Urine Test

DNA Labs UAE is a leading facility in the field of genetic and molecular testing, offering a wide range of services to help individuals understand their health better. Among the various tests offered, the Metal Screen 3 Urine Test stands out for its importance in detecting heavy metal exposure, which is crucial for preventing and […]

Symptoms and Testing information for PTH Antibody Test

Symptoms and Testing information for PTH Antibody Test

In the realm of medical diagnostics, the PTH Antibody Test stands out as a crucial examination for individuals experiencing symptoms related to parathyroid disorders. DNA Labs UAE, a leading genetic laboratory, offers this comprehensive test, providing essential insights into the health of the parathyroid glands. Understanding the symptoms that necessitate this test, its significance, and […]

Symptoms and Testing information for Duchenne Becker Muscular Dystrophy DMD BMD Gene Mutation Test

Symptoms and Testing information for Duchenne Becker Muscular Dystrophy DMD BMD Gene Mutation Test

Symptoms of Duchenne Becker Muscular Dystrophy (DMD/BMD) and the Importance of Gene Mutation Testing Duchenne and Becker Muscular Dystrophy (DMD/BMD) are two forms of muscular dystrophy, genetic disorders characterized by progressive muscle degeneration and weakness. Caused by mutations in the dystrophin gene, which is essential for maintaining muscle cell structure, DMD and BMD vary in […]

Symptoms and Testing information for Spinal Muscular Atrophy SMA Carrier Detection Test

Symptoms and Testing information for Spinal Muscular Atrophy SMA Carrier Detection Test

Spinal Muscular Atrophy (SMA) is a genetic disorder characterized by weakness and wasting (atrophy) in muscles used for movement. It results from the loss of specialized nerve cells, called motor neurons, in the spinal cord and the part of the brain that is connected to the spinal cord. SMA affects individuals differently, but the common […]

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