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 […]
Growth Hormone Receptor (GHRHR) gene mutations can lead to growth hormone deficiency (GHD), a condition that affects both children and adults, with a wide range of symptoms and implications for health. At DNA Labs UAE, we offer a comprehensive genetic test specifically designed to diagnose mutations in the GHRHR gene. This test is crucial for […]
— Symptoms of STAT5B Gene Growth Hormone Insensitivity with Immunodeficiency Genetic Test The STAT5B gene plays a crucial role in the human body, influencing growth, development, and the immune system’s functionality. Mutations in the STAT5B gene can lead to growth hormone insensitivity accompanied by immunodeficiency, a rare but significant condition. DNA Labs UAE offers a […]
Hemolytic Uremic Syndrome (HUS) is a rare condition that affects the blood and blood vessels. It results in the destruction of blood platelets (cells involved in clotting), a low red blood cell count (anemia), and kidney failure due to damage to the very small blood vessels of the kidneys. Some forms of HUS are genetically […]
Hemolytic Uremic Syndrome (HUS) is a severe condition characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal failure. A significant subtype of this syndrome, known as atypical HUS (aHUS), is primarily caused by genetic mutations, including those in the CFH (Complement Factor H) gene. Understanding the symptoms and the importance of genetic testing […]
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.
