Lipodystrophy Type 2, also known as Familial Partial Lipodystrophy (FPLD2), is a rare genetic disorder characterized by the abnormal distribution of fat in the body. This condition is specifically associated with mutations in the LMNA gene. Individuals with FPLD2 typically experience a loss of subcutaneous fat from the arms, legs, and trunk, which may lead […]
Lipodystrophy is a rare disorder characterized by the abnormal distribution of body fat. Generalized Lipodystrophy Type 4, also known as CAVIN1 gene lipodystrophy, is a particularly rare form that affects individuals from an early age. DNA Labs UAE is at the forefront of diagnosing this condition through the CAVIN1 Gene Lipodystrophy Generalized Type 4 Genetic […]
Lipodystrophy is a rare condition characterized by the abnormal distribution of fat in the body. Among its types, Generalized Lipodystrophy Type 2, also known as Berardinelli-Seip Congenital Lipodystrophy Type 2 (BSCL2), is particularly notable for its genetic roots. This condition is caused by mutations in the BSCL2 gene, leading to a wide range of symptoms […]
In the rapidly advancing field of genetics, identifying and understanding the genetic basis of diseases has become crucial for effective diagnosis and management. One such condition, AGPAT2 Gene Lipodystrophy Generalized Type 1, has garnered attention due to its significant impact on individuals’ health. DNA Labs UAE is at the forefront of providing comprehensive genetic testing […]
Symptoms of ITGB2 Gene Leukocyte Adhesion Deficiency Genetic Test Leukocyte Adhesion Deficiency (LAD) is a rare, autosomal recessive immune disorder caused by mutations in the ITGB2 gene. This gene plays a crucial role in the immune system, particularly in the process of leukocyte (white blood cells) adhesion and migration. Mutations in the ITGB2 gene lead […]
Leukocyte Adhesion Deficiency (LAD) is a rare, autosomal recessive immune disorder that affects the body’s ability to combat infections. The ITGB1 gene plays a pivotal role in this condition, and genetic testing for mutations in this gene can provide crucial information for diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for the […]
Understanding LCAT Gene Deficiency LCAT (Lecithin-Cholesterol Acyltransferase) deficiency is a rare genetic disorder that affects the body’s ability to metabolize lipids properly. This condition is caused by mutations in the LCAT gene, leading to various systemic and ocular symptoms. Understanding the symptoms and getting a timely diagnosis can significantly improve the quality of life for […]
In the realm of genetic testing, understanding the nuances of specific gene deficiencies is crucial for early diagnosis and treatment. Among these, the ACADL gene, associated with Long-Chain Acyl-CoA Dehydrogenase (LCAD) deficiency, plays a significant role in how the body metabolizes fats. This article delves into the symptoms of ACADL gene LCAD deficiency, the importance […]
Lactose intolerance is a common digestive problem where the body is unable to digest lactose, a type of sugar mainly found in milk and dairy products. Symptoms can range from mild to severe and can significantly impact an individual’s quality of life. Understanding the genetic basis of lactose intolerance can provide valuable insights into managing […]
Lactic acidemia, a condition characterized by an elevated level of lactate in the blood, can be a symptom of various underlying metabolic disorders. One such disorder is PDHX gene-related lactic acidemia due to PDX1 deficiency. This genetic condition is rare and often requires specific testing for accurate diagnosis and management. DNA Labs UAE offers a […]
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.
