Symptoms of BCR-ABL1 Kinase Domain Mutation Analysis IRMA Test The BCR-ABL1 Kinase Domain Mutation Analysis IRMA Test is a critical diagnostic tool used in the field of genetic medicine, particularly in the monitoring and treatment planning for patients with certain types of leukemia. This test specifically targets mutations in the BCR-ABL1 gene, which are a […]
Genetic Diseases
Symptoms and Testing information for Spinal Muscular Atrophy Carrier Screening Test
Spinal Muscular Atrophy (SMA) is a severe genetic disorder that affects the motor neurons in the spinal cord, leading to muscle wasting and weakness. While individuals with SMA show symptoms, carriers of the genetic mutation responsible for SMA often do not. However, when two carriers have a child, there’s a 25% chance the child will […]
Symptoms and Testing information for Spinal Muscular Atrophy Screening Prenatal Test
Spinal Muscular Atrophy (SMA) is a genetic disorder that affects the control of muscle movement. It is caused by a 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. The loss of these neurons leads to muscle weakness and […]
Symptoms and Testing information for Peace of Mind Father Child Test
In the realm of genetic testing, the bond between a father and a child is one of the most profound connections that can be explored and confirmed. DNA Labs UAE is at the forefront of providing accurate, confidential, and reliable DNA testing services to families seeking clarity and peace of mind. Among the various tests […]
Symptoms and Testing information for Complement-Dependent Cytotoxicity CDC Crossmatch Test
At DNA Labs UAE, we understand the critical importance of accurate diagnostic procedures in the management and treatment of various medical conditions. One such pivotal diagnostic test we offer is the Complement-Dependent Cytotoxicity (CDC) Crossmatch Test. This test plays a crucial role in the pre-transplant evaluation process, ensuring compatibility between donor and recipient, thereby reducing […]
Symptoms and Testing information for Prenatal Diagnostic Screening by Karyotyping Test
Prenatal diagnostic screening is a crucial step in assessing the health and development of a fetus. Among the various methods available, karyotyping tests have emerged as a vital tool for detecting chromosomal abnormalities that could lead to genetic disorders. DNA Labs UAE, a leading genetic laboratory, offers comprehensive prenatal diagnostic screening through karyotyping tests to […]
Symptoms and Testing information for QF PCR Panel 131821XY and Karyotyping Test
DNA Labs UAE is at the forefront of genetic testing and analysis, offering a comprehensive range of services designed to provide individuals with crucial information about their genetic makeup. Among the various tests available, the QF PCR Panel 131821XY and Karyotyping Test stands out as a pivotal diagnostic tool for detecting chromosomal abnormalities that can […]
Symptoms and Testing information for Chromosome Interphase Profiling Products of Conception Test
Understanding the genetic health of a fetus is a crucial part of prenatal care, and it is an area where modern medicine has made significant strides. One of the advanced tests available for this purpose is the Chromosome Interphase Profiling Products of Conception Test. This test is particularly important for couples who have experienced miscarriages, […]
Symptoms and Testing information for Thalassemia Alpha Trio Prenatal Mutation Detection Test
In the realm of genetic testing and diagnostics, understanding the intricacies of various genetic conditions is pivotal for early detection and management. Thalassemia, a blood disorder passed down through families, is one such condition that significantly impacts the body’s ability to produce hemoglobin, leading to anemia. The Thalassemia Alpha Trio Prenatal Mutation Detection Test is […]
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 […]