Symptoms and Testing information for VNTR Chimerism Study PRE BMT Test

Symptoms and Testing information for VNTR Chimerism Study PRE BMT Test

Understanding the Symptoms of VNTR Chimerism Study Pre BMT Test Variable Number Tandem Repeat (VNTR) chimerism studies are pivotal in the realm of bone marrow transplantation (BMT), offering insights that are crucial for the success of the procedure. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the VNTR Chimerism […]

Symptoms and Testing information for Y Chromosome Microdeletion 16 Mutations Test

Symptoms and Testing information for Y Chromosome Microdeletion 16 Mutations Test

Y Chromosome Microdeletion is a genetic condition that can significantly impact male fertility. This condition is characterized by missing genes on the Y chromosome, which is one of the two sex chromosomes in males (XY). The Y Chromosome Microdeletion 16 Mutations Test is a critical diagnostic tool used to identify specific deletions on the Y […]

Symptoms and Testing information for NUDT15 Gene Mutation Analysis Test

Symptoms and Testing information for NUDT15 Gene Mutation Analysis Test

DNA labs UAE is at the forefront of genetic testing and personalized medicine, offering a comprehensive range of analyses to understand better the genetic makeup of individuals. Among these, the NUDT15 gene mutation analysis test stands out due to its significant implications for medication metabolism and the risk of adverse drug reactions. Understanding the symptoms […]

Symptoms and Testing information for Prenatal Alpha Thalassemia Mutation Screening 3 Common Mutation Test

Symptoms and Testing information for Prenatal Alpha Thalassemia Mutation Screening 3 Common Mutation Test

Understanding Prenatal Alpha Thalassemia Mutation Screening Alpha Thalassemia is a genetic blood disorder affecting the production of hemoglobin, the protein in red blood cells responsible for carrying oxygen throughout the body. This condition can lead to anemia, jaundice, and more severe health complications if not diagnosed early. The prenatal alpha thalassemia mutation screening, specifically targeting […]

Symptoms and Testing information for Beta Thalassemia-9 Common Mutations Screening Couple Test

Symptoms and Testing information for Beta Thalassemia-9 Common Mutations Screening Couple Test

Beta Thalassemia is a genetic blood disorder that reduces the production of hemoglobin, the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. Individuals with this condition experience an array of symptoms that can significantly impact their quality of life. Recognizing these symptoms early on is crucial for managing the […]

Symptoms and Testing information for Beta Thalassemia-HBB Full Gene Analysis Single Test

Symptoms and Testing information for Beta Thalassemia-HBB Full Gene Analysis Single Test

Beta Thalassemia is a blood disorder that diminishes the production of hemoglobin, an iron-containing protein in red blood cells that carries oxygen to cells throughout the body. It is a genetic condition that involves the mutation of the HBB gene on chromosome 11, often leading to severe anemia, a condition where the body doesn’t have […]

Symptoms and Testing information for cKIT Mutation Screening Exons 9 11 13 17 AML Test

Symptoms and Testing information for cKIT Mutation Screening Exons 9 11 13 17 AML Test

Understanding the implications of genetic mutations is crucial in the realm of medical science, especially when it comes to diagnosing and treating various types of cancers. One such mutation that has garnered attention is the cKIT mutation, particularly in the context of Acute Myeloid Leukemia (AML). DNA Labs UAE is at the forefront of providing […]

Symptoms and Testing information for Cystic Fibrosis Mutation Screening CFTR - Del 508 G551DR553X G542X Test

Symptoms and Testing information for Cystic Fibrosis Mutation Screening CFTR – Del 508 G551DR553X G542X Test

Cystic fibrosis (CF) is a severe genetic disorder that affects the lungs, digestive system, and other organs. It results from mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene, which leads to the production of thick, sticky mucus that can clog the airways and trap bacteria, leading to infections, inflammation, and other complications. Among […]

Symptoms and Testing information for Prenatal Delta Beta- Thalassaemia Mutation Screening Test

Symptoms and Testing information for Prenatal Delta Beta- Thalassaemia Mutation Screening Test

Symptoms of Prenatal Delta Beta-Thalassaemia Mutation Screening Test Delta Beta-Thalassaemia is a rare blood disorder that results from mutations affecting the production of hemoglobin, the protein in red blood cells responsible for carrying oxygen throughout the body. This condition can lead to anemia and other health issues, making early detection crucial for effective management. DNA […]

Symptoms and Testing information for DMD BMD Mutation Screening 26 Exons Test

Symptoms and Testing information for DMD BMD Mutation Screening 26 Exons Test

Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are two forms of muscular dystrophy that are caused by mutations in the dystrophin gene. These conditions lead to muscle weakness and degeneration over time. The DMD/BMD Mutation Screening 26 Exons Test is a specialized genetic test designed to identify mutations in the 26 exons of […]

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