DNA Labs UAE stands at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into various genetic conditions. Among these, the THBD Gene Hemolytic Uremic Syndrome Genetic Test is a critical tool for diagnosing Hemolytic Uremic Syndrome (HUS), a rare but severe condition that affects the blood and blood […]
Glycine encephalopathy, also known as non-ketotic hyperglycinemia, is a rare genetic disorder that affects the body’s ability to break down the amino acid glycine. This condition results from mutations in several genes, including the AMT gene, which plays a crucial role in the glycine cleavage system. Due to the complexity and rarity of this condition, […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive genetic testing services to aid in the diagnosis and management of various genetic conditions. One such condition is the Atypical Hemolytic Uremic Syndrome (aHUS), specifically associated with mutations in the CD46 gene, which leads to a susceptibility to Atypical Hemolytic Uremic Syndrome […]
Glycine encephalopathy, also known as non-ketotic hyperglycinemia (NKH), is a rare genetic disorder affecting the body’s ability to break down the amino acid glycine. This condition results from mutations in several genes, including the GLDC gene. DNA Labs UAE offers a comprehensive genetic test for those concerned about this condition, providing essential insights into your […]
The SCO1 gene is critical for the proper functioning of the human body, playing a pivotal role in the assembly of cytochrome c oxidase, an essential component of the mitochondrial respiratory chain. Mutations in the SCO1 gene can lead to severe disorders, notably early onset hepatic failure and neurologic disorder. Understanding the symptoms of this […]
Genetic testing has become a cornerstone in the diagnosis and understanding of numerous inherited disorders, enabling healthcare professionals and patients alike to navigate the complexities of genetic conditions with greater accuracy. One such condition that has garnered attention is the deficiency in the Glycine N-Methyltransferase (GNMT) gene. This article delves into the symptoms associated with […]
Hepatic Venoocclusive Disease with Immunodeficiency (VODI) is a rare genetic disorder that poses significant health risks to affected individuals. This condition is caused by mutations in the SP110 gene, which plays a critical role in immune system function and liver health. Understanding the symptoms of this disorder is crucial for early diagnosis and management. At […]
The KEAP1 gene plays a significant role in the body’s defense against oxidative stress. Mutations in this gene have been linked to various health conditions, including the development of goitre, specifically the multilnodular type. Goitre is a condition characterized by an abnormal enlargement of the thyroid gland. While it can result from several factors, genetic […]
Symptoms of KCNJ5 Gene Hyperaldosteronism Type 3 Genetic Test Hyperaldosteronism, a condition characterized by the overproduction of aldosterone by the adrenal glands, can lead to a range of health issues, including high blood pressure, muscle weakness, and potassium deficiency. Type 3 hyperaldosteronism, specifically linked to mutations in the KCNJ5 gene, is a rare and severe […]
Understanding GH1 Gene Growth Hormone Deficiency Growth Hormone Deficiency (GHD) is a rare condition that can affect both children and adults, leading to a variety of health issues. At the heart of this condition is the GH1 gene, which plays a crucial role in the production of growth hormone. This hormone is essential for stimulating […]
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.
