Hemochromatosis is a genetic condition characterized by excessive iron accumulation in the body, leading to various health issues. Type 4 Hemochromatosis, also known as Ferroportin Disease, is caused by mutations in the SLC40A1 gene. This particular type of hemochromatosis is autosomal dominant, meaning that inheriting a single copy of the mutated gene from one parent […]
— Hypercholesterolemia, particularly Familial Hypercholesterolemia (FH), is a critical condition that significantly increases the risk of coronary heart disease. Among the genetic variants causing this condition, mutations in the LDLRAP1 gene result in a form of autosomal recessive hypercholesterolemia. Understanding the symptoms and undergoing genetic testing for the LDLRAP1 gene can be crucial in managing […]
G6PD deficiency is a genetic disorder that affects the red blood cells, leading to a condition known as hemolytic anemia. This condition is particularly prevalent in certain parts of the world, including the Middle East. Understanding the symptoms and undergoing genetic testing can be crucial for managing the condition effectively. DNA Labs UAE offers a […]
Understanding GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Glucose Phosphate Isomerase (GPI) deficiency is a rare genetic disorder that affects the way red blood cells function, leading to a form of hemolytic anemia known as GPI Gene Hemolytic Anemia Nonspherocytic. This condition is caused by mutations in the GPI gene, which […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that cater to a wide range of genetic conditions, including Hemophilia A. Hemophilia A is a serious genetic disorder that impairs the body’s ability to make blood clots, a process needed to stop bleeding. This condition is caused by a deficiency in […]
In the realm of genetic testing, understanding the nuances of our genetic makeup can provide invaluable insights into our health and predispositions to certain conditions. One such area of interest lies in the examination of the CETP gene and its impact on high-density lipoprotein (HDL) cholesterol levels. At DNA Labs UAE, we offer a comprehensive […]
Holocarboxylase Synthetase (HLCS) deficiency is a rare genetic condition that affects the body’s ability to process certain proteins properly. This condition is caused by mutations in the HLCS gene, which plays a crucial role in the metabolism of several essential nutrients. Individuals with HLCS deficiency have difficulty converting certain forms of B-vitamins into their active […]
In the realm of genetic testing, advancements have paved the way for the early detection and understanding of various genetic disorders, one of which is Hurler Syndrome. This condition, rooted in the IDUA gene, can have profound implications on an individual’s health and quality of life. DNA Labs UAE stands at the forefront of these […]
Understanding the complexities of genetic disorders is crucial in the realm of medical science. One such disorder is the Hurler-Scheie Syndrome, which stems from mutations in the IDUA gene. This article delves into the symptoms of this condition, the significance of genetic testing, and details about the IDUA Gene Hurler-Scheie Syndrome Genetic Test available at […]
Guanidinoacetate Methyltransferase (GAMT) deficiency is a rare disorder that affects the body’s ability to produce creatine, a molecule crucial for energy storage in cells, particularly in the brain and muscles. This genetic condition, caused by mutations in the GAMT gene, can lead to a range of neurological and physical symptoms. Recognizing these symptoms early can […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
