Blogs

Genetic testing has become a cornerstone in the diagnosis and understanding of various genetic disorders. One such condition, which is rare but significant, is the deficiency of 3-Hydroxyisobutryl-CoA Hydrolase, stemming from mutations in the HIBCH gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the HIBCH Gene 3-Hydroxyisobutryl-CoA Hydrolase […]

Symptoms of HADH Gene 3-Hydroxyacyl-CoA Dehydrogenase Deficiency 3-Hydroxyacyl-CoA dehydrogenase (HADH) deficiency is a rare genetic disorder that impacts the body’s ability to metabolize certain fats into energy, especially during periods of fasting. This condition, also known as hyperinsulinism-hyperammonemia syndrome, can lead to a variety of symptoms, which may vary significantly among individuals. Recognizing these symptoms […]

Understanding the symptoms of HMGCS2 gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 deficiency is crucial for early diagnosis and management of the condition. This genetic disorder affects the body’s ability to produce ketones, which are an important source of energy during periods of fasting. At DNA Labs UAE, we provide a comprehensive genetic test for this condition, which […]

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 […]

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 […]

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 […]

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 […]

— 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 […]

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 intricacies of our genetic makeup can unlock answers to numerous health-related questions, especially when it comes to identifying the root causes of certain conditions. One such genetic factor is the CYP17A1 gene, which plays a critical role in the body’s steroidogenesis process. Deficiencies in the 17-Hydroxylation activity of this gene can lead to […]