Blogs

Symptoms and Testing information for Non-Invasive Prenatal Testing Yes-In-Gene Test

Symptoms and Testing information for Non-Invasive Prenatal Testing Yes-In-Gene Test

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 […]

Symptoms and Testing information for Microsatellite Instability Lynch Syndrome Colorectal Cancer Test

Symptoms and Testing information for Microsatellite Instability Lynch Syndrome Colorectal Cancer Test

Microsatellite Instability (MSI) is a condition often linked to Lynch Syndrome, a genetic disorder that significantly increases the risk of developing colorectal cancer among other types of cancer. Lynch Syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC), is the most common hereditary form of colorectal cancer. Individuals with Lynch Syndrome have a higher risk […]

Symptoms and Testing information for Microarray 60K POCand Single Karyotyping Test

Symptoms and Testing information for Microarray 60K POCand Single Karyotyping Test

In the realm of genetic diagnostics and personalized medicine, the Microarray 60K POC and Single Karyotyping Test stands out as a sophisticated tool designed to detect a wide range of genetic abnormalities. This comprehensive test, offered by DNA Labs UAE, provides invaluable insights into genetic disorders, enabling healthcare professionals to devise personalized treatment plans for […]

Symptoms and Testing information for MECP2 Full Gene Mutation Analysis Rett Syndrome Test

Symptoms and Testing information for MECP2 Full Gene Mutation Analysis Rett Syndrome Test

Symptoms of MECP2 Full Gene Mutation Analysis Rett Syndrome Test Rett Syndrome is a rare, severe neurological disorder that primarily affects females. It leads to severe impairments, affecting nearly every aspect of the child’s life: their ability to speak, walk, eat, and even breathe easily. The key to managing Rett Syndrome lies in its early […]

Symptoms and Testing information for Liquid Bx. Cell-Free EGFR T790ML858R Exon 19 Deletion Test

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 […]

Symptoms and Testing information for DMD Mutation Screening 79 Exons Prenatal Test

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 CAH Congenital Adrenal Hyperplasia Full Gene Sequence Analysis Test

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 Beta Thalassemia-HBB Full Gene Analysis Couple Test

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 BCR-ABL1 Kinase Domain Mutation Analysis IRMA Test

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 Microsatellite Instability MSI PCR Test

Symptoms and Testing information for Microsatellite Instability MSI PCR Test

Understanding Microsatellite Instability (MSI) and Its Importance Microsatellite Instability (MSI) is a condition that can be indicative of certain types of cancers, particularly colorectal cancer. It is a change that occurs in the DNA of some cancer cells, where the number of short, repeated sequences of DNA, known as microsatellites, changes as a result of […]

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