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 […]
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 […]
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 […]
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 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 fat in the body. Among its various types, Familial Partial Lipodystrophy (FPLD) is notable for its genetic basis, and within this category, the PPARG gene plays a critical role in the development of Type 3 Familial Partial Lipodystrophy (FPLD3). Understanding the symptoms and […]
Symptoms of HADHA Gene Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency Genetic Test Understanding the genetic basis of metabolic disorders is crucial for early diagnosis and management. One such condition, Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency, is a rare metabolic disorder affecting the body’s ability to oxidize fatty acids into energy. This condition is caused by mutations in the […]
In the realm of genetic diagnostics, understanding the intricacies of our genetic makeup has become increasingly accessible and informative, offering insights into conditions that were once shrouded in mystery. Among these conditions is the deficiency in the LPA gene, a concern that has garnered attention for its potential implications on health. DNA Labs UAE, a […]
In the rapidly advancing field of genetic diagnostics, understanding the nuances of specific gene deficiencies is crucial for the early detection and management of inherited conditions. One such condition is the deficiency of the ABHD1 gene, which affects the lung’s alpha-beta hydrolase enzyme. This article aims to shed light on the symptoms associated with ABHD1 […]
Understanding ACP2 Gene Lysosomal Acid Phosphatase Deficiency Lysosomal acid phosphatase deficiency, linked to mutations in the ACP2 gene, is a rare genetic disorder that can lead to a variety of health issues. The ACP2 gene plays a crucial role in the body, encoding an enzyme necessary for breaking down certain molecules within the lysosomes. Lysosomes […]
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.
