Symptoms of DMGDH Gene Dimethylglycine Dehydrogenase Deficiency Dimethylglycine Dehydrogenase (DMGDH) deficiency is a rare genetic disorder that affects the body’s ability to metabolize certain amino acids properly. This condition can lead to a variety of health issues, ranging from mild to severe. Recognizing the symptoms early can be crucial for managing the condition effectively. Some […]
Symptoms of DYM Gene Dyggve-Melchior-Clausen Disease Dyggve-Melchior-Clausen (DMC) disease is a rare genetic disorder that affects bone development and structure, leading to skeletal dysplasia. This condition is caused by mutations in the DYM gene, which plays a crucial role in the development and maintenance of healthy bone and cartilage. Individuals with DMC disease exhibit a […]
Symptoms of CYP2B6 Gene Efavirenz Poor Metabolism of Genetic Test The CYP2B6 gene plays a pivotal role in the metabolism of various substances within the body, including the antiretroviral medication, Efavirenz, which is commonly used in the treatment of HIV. Variations in the CYP2B6 gene can lead to poor metabolism of Efavirenz, resulting in higher […]
Symptoms of TMPRSS15 Gene Enterokinase Deficiency Genetic Test The TMPRSS15 gene plays a crucial role in the human body, encoding for the enzyme enterokinase, which is essential for the digestion of proteins. A deficiency in this gene can lead to a range of symptoms and health issues, necessitating accurate diagnosis and management. DNA Labs UAE […]
Genetic testing has become a cornerstone in the diagnosis and management of various inherited disorders. Among these, the SLC16A1 gene erythrocyte lactate transporter defect is a condition that has garnered attention due to its impact on lactate transport in red blood cells. This article provides an in-depth look at the symptoms associated with this genetic […]
In the realm of genetic diagnostics and personalized medicine, understanding the nuances of specific genetic conditions is paramount. One such condition, Fabry disease, caused by mutations in the GLA gene, has garnered significant attention due to its wide range of symptoms and the critical importance of early detection. DNA Labs UAE stands at the forefront […]
Symptoms of F2 Gene Factor II Deficiency Genetic Test Understanding the genetic underpinnings of our health is more critical than ever, especially with conditions that might not be immediately apparent. One such condition is Factor II deficiency, a rare blood clotting disorder. It’s essential to recognize the symptoms of this condition early on, and the […]
Understanding the Symptoms of F5 Gene Factor V Deficiency Factor V deficiency, also known as Owren’s disease or parahemophilia, is a rare genetic disorder that affects the blood’s ability to clot. This condition is caused by mutations in the F5 gene, which plays a crucial role in the coagulation system. Recognizing the symptoms of F5 […]
Understanding F13B Gene Factor XIIIB Deficiency Factor XIII deficiency, specifically related to the F13B gene, is a rare genetic disorder that affects the blood’s clotting ability. This condition, resulting from mutations in the F13B gene, can lead to excessive bleeding or bruising, even from minor injuries. Understanding the symptoms and undergoing genetic testing can help […]
Cystinosis is a rare, inherited metabolic disorder characterized by the accumulation of cystine within the cells. This accumulation leads to the formation of crystals that can cause damage to various organs and tissues, particularly the kidneys. The CTNS gene is responsible for this condition, and mutations in this gene lead to the different forms of […]
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.
