In the realm of prenatal care, the advent of non-invasive prenatal testing (NIPT) has been a game-changer, offering expectant parents a safer, more accurate glimpse into the genetic health of their unborn child. Among these advancements, the Yes-In-Gene Test stands out for its comprehensive screening capabilities. Offered by DNA Labs UAE, this test is designed […]
Genetic Diseases
Symptoms and Testing information for PDGFR and cKIT Gastrointestinal Stromal Tumors Test
Gastrointestinal stromal tumors (GISTs) represent a unique subset of cancers that originate from the digestive tract’s connective tissue or, less frequently, from the omentum, mesentery, or retroperitoneum. The discovery of mutations in the Platelet-Derived Growth Factor Receptor Alpha (PDGFRA) and the proto-oncogene cKIT (CD117) has significantly advanced our understanding of the pathogenesis of these tumors. […]
Symptoms and Testing information for Prenatal Hemophilia A Common Mutation Screening Factor VIII Intron 22 and Intron 1 Inversion Analysis Test
Hemophilia A is a genetic disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. This condition can lead to excessive bleeding following an injury or surgery. Hemophilia A is primarily caused by mutations in the Factor VIII gene. Among these, the inversion of intron 22 and intron 1 […]
Symptoms and Testing information for Spino Cerebral Ataxia SCA Panel – 1 2 3 6 7 10 and 12 Test
Spinocerebellar ataxia (SCA) represents a group of hereditary ataxias that are characterized by degenerative changes in the part of the brain related to the control of movement, and in some cases, in the spinal cord. There are many types of SCA, and they are classified according to the mutated gene responsible for the disorder. Among […]
Symptoms and Testing information for Molecular Karyotyping for Amniotic Fluid Test
In the realm of prenatal diagnostics, the advancement of genetic testing has opened up new avenues for expecting parents to gain insights into their unborn child’s health. Among these tests, Molecular Karyotyping for Amniotic Fluid Test stands out as a comprehensive method to detect chromosomal abnormalities. Conducted at DNA Labs UAE, this test is pivotal […]
Symptoms and Testing information for BCR-ABL1 Kinase Domain Mutation Analysis IRMA Test
DNA Labs UAE is a premier genetic testing facility that offers a wide range of diagnostic services to help patients understand their genetic makeup and potential health risks. Among the various tests provided, the BCR-ABL1 Kinase Domain Mutation Analysis IRMA Test stands out for its critical role in the management of certain types of leukemia. […]
Symptoms and Testing information for Beta Thalassemia-HBB Full Gene Analysis Couple Test
Beta Thalassemia is a blood disorder that reduces the production of hemoglobin, an iron-containing protein in red blood cells that enables them to carry oxygen. This genetic condition can lead to anemia, a deficiency in the number and quality of red blood cells. The severity of Beta Thalassemia varies; some individuals might experience mild symptoms […]
Symptoms and Testing information for CAH Congenital Adrenal Hyperplasia Full Gene Sequence Analysis Test
Understanding Congenital Adrenal Hyperplasia (CAH) Congenital Adrenal Hyperplasia (CAH) is a genetic disorder that affects the adrenal glands, leading to a production imbalance of adrenal hormones such as cortisol, aldosterone, and androgens. This imbalance can cause a range of symptoms and health issues, varying in severity from non-classic (mild) to classic (severe) forms of the […]
Symptoms and Testing information for DMD Mutation Screening 79 Exons Prenatal Test
— Duchenne Muscular Dystrophy (DMD) is a severe type of muscular dystrophy that primarily affects boys. It is a genetic disorder characterized by progressive muscle degeneration and weakness. DMD is caused by mutations in the DMD gene, which is responsible for the production of dystrophin, a protein essential for maintaining muscle cell structure. Early diagnosis […]
Symptoms and Testing information for Liquid Bx. Cell-Free EGFR T790ML858R Exon 19 Deletion Test
In the ever-evolving field of genetic testing, one of the most significant advancements has been the development of liquid biopsy (Liquid Bx.) techniques. These innovative methods allow for the non-invasive detection of genetic mutations from circulating tumor DNA (ctDNA) in blood samples. Among these, the Cell-Free EGFR T790M/L858R Exon 19 Deletion Test stands out for […]