Metabolic Disorders

Understanding the intricacies of our genetic makeup can be a gateway to personalized healthcare and preventive strategies against numerous diseases. One such genetic marker that has garnered attention in the medical community is the DECR1 gene, known for its role in fatty acid metabolism. The DECR1 gene, encoding the 24-Dienoyl-CoA Reductase 1 enzyme, plays a […]

— Understanding the symptoms of NADK2 Gene 24-Dienoyl-CoA Reductase Deficiency is crucial for early diagnosis and management of this rare genetic disorder. DNA Labs UAE offers a comprehensive genetic test for this condition, aimed at providing essential insights into your genetic health. NADK2 Gene 24-Dienoyl-CoA Reductase Deficiency is a rare metabolic disorder that affects the […]

DNA Labs UAE is at the forefront of genetic testing and analysis, offering a comprehensive range of services designed to provide individuals with critical insights into their genetic makeup. Among these, the DHTKD1 Gene 2-Aminoadipic 2-Oxoadipic Aciduria Genetic Test stands out for its significance in diagnosing a rare metabolic disorder. This condition is characterized by […]

ACADSB, or Acyl-CoA Dehydrogenase Short/Branched Chain, is a gene that plays a crucial role in the metabolic pathway that breaks down certain amino acids and fatty acids to produce energy. Mutations in the ACADSB gene can lead to a rare metabolic disorder known as 2-Methylbutyrylglycinuria. This condition can lead to various health issues, and early […]

The HSD3B2 gene plays a crucial role in the production of hormones in the body. It is involved in the biosynthesis of all classes of steroid hormones, including glucocorticoids, mineralocorticoids, and sex steroids. Deficiency in the enzyme 3-beta-hydroxysteroid dehydrogenase, due to mutations in the HSD3B2 gene, can lead to a rare disorder known as 3-Beta-Hydroxysteroid […]

In the realm of genetic diagnostics, the detection and understanding of rare metabolic disorders are critical for timely intervention and management. One such condition, 3-Hydroxy-3-Methylglutaryl-CoA Lyase (HMGCL) deficiency, is a rare but serious metabolic disorder that can lead to significant health issues if not identified and managed appropriately. DNA Labs UAE is at the forefront […]

Understanding the Symptoms of Infliximab Antibody Test Infliximab is a powerful medication used in the treatment of various autoimmune diseases, including Crohn’s disease, rheumatoid arthritis, ulcerative colitis, psoriasis, and ankylosing spondylitis. While it offers significant relief for many patients, the body can sometimes develop antibodies against infliximab, reducing its effectiveness and necessitating monitoring through an […]

At DNA Labs UAE, we understand the critical importance of accurate and timely health diagnostics. One such diagnostic test that has garnered attention for its role in managing autoimmune diseases is the Infliximab Anti-TNF Blocker Test. This test is crucial for individuals undergoing treatment with Infliximab, a medication used to suppress the immune system’s activity […]

Understanding the Symptoms Addressed by the Newborns Genetic Test Panel NGS Genetic Test In the realm of medical advancements, genetic testing stands out as a beacon of hope for early diagnosis and intervention, particularly in newborns. DNA Labs UAE is at the forefront of this innovation, offering a comprehensive Newborns Genetic Test Panel through Next-Generation […]

Lysosomal storage disorders (LSDs) represent a group of over 50 genetically inherited conditions that are characterized by an abnormal build-up of various toxic materials in the body’s cells as a result of enzyme deficiencies. These disorders are caused by mutations in the genes that encode enzymes responsible for the breakdown of certain substances within the […]