Isobutyryl-CoA Dehydrogenase Deficiency, caused by mutations in the ACAD8 gene, is a rare metabolic disorder that affects the body’s ability to process certain fats. This condition, although rare, can lead to a variety of symptoms and health issues, ranging from mild to severe. DNA Labs UAE offers a genetic test specifically designed to detect mutations […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that cater to a wide range of conditions, ensuring that individuals and families have access to crucial health information. One such condition that we specialize in testing for is Isovaleric Acidemia (IVA), a rare genetic disorder that can have significant impacts on […]
Krabbe Disease, also known as globoid cell leukodystrophy, is a rare, inherited disorder that affects the nervous system. It is caused by mutations in the GALC gene, which leads to a deficiency in an enzyme essential for the metabolism of certain lipids in the body. This deficiency results in the accumulation of toxic substances in […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide insights into your genetic makeup and health predispositions. Among the various tests offered, the FXYD2 Gene Hypomagnesemia Type 2 Genetic Test is a critical tool for diagnosing a rare but significant condition that affects […]
Krabbe disease, also known as globoid cell leukodystrophy, is a rare and often devastating genetic disorder that affects the nervous system. It results from the deficiency of an essential enzyme, leading to the accumulation of certain lipids, which in turn damages the myelin sheath, the protective covering of nerve cells. This disease is primarily inherited […]
Symptoms of CLDN16 Gene Hypomagnesemia Type 3 Genetic Test Hypomagnesemia type 3, caused by mutations in the CLDN16 gene, is a rare genetic disorder that can significantly impact an individual’s health. Understanding the symptoms of this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers a comprehensive genetic test for this condition, […]
L-2-hydroxyglutaric aciduria (L2HGA) is a rare, inherited metabolic disorder characterized by the accumulation of L-2-hydroxyglutaric acid in the body. This condition is caused by mutations in the L2HGDH gene, which plays a crucial role in the metabolism of certain amino acids. Understanding the symptoms and the importance of genetic testing for this condition is vital […]
Understanding the intricacies of our genetic makeup is crucial in diagnosing and managing various health conditions. One such condition that has garnered attention is Hypomagnesemia Type 4, linked to mutations in the EGF gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the EGF Gene Hypomagnesemia Type 4 Genetic […]
Lactose intolerance is a common condition that affects millions of people worldwide. It is caused by a deficiency in lactase, the enzyme responsible for breaking down lactose, a sugar found in milk and dairy products. The symptoms can range from mild discomfort to severe gastrointestinal distress. Understanding the genetic basis of lactose intolerance can help […]
In the realm of genetic testing, understanding the intricacies of specific conditions is crucial for early diagnosis and effective management. One such condition that has garnered attention is Hypomagnesemia Type 5, caused by mutations in the CLDN19 gene. This article delves into the symptoms associated with this condition, the significance of the CLDN19 gene Hypomagnesemia […]
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.
