Methylmalonic Aciduria (MMA) CblF type is a rare genetic disorder that affects the body’s ability to process certain parts of proteins and fats properly. This condition is caused by mutations in the LMBRD1 gene, leading to a deficiency in the synthesis of a protein essential for vitamin B12 metabolism. The inability to metabolize vitamin B12 […]
Methylmalonic aciduria and homocystinuria, cblD type, is a rare genetic disorder that arises from mutations in the MMADHC gene. This condition can lead to a variety of health issues, ranging from mild to severe. It is part of a group of disorders that affect the metabolism of certain parts of vitamins (like vitamin B12) which […]
Methylmalonic aciduria CblC type, caused by mutations in the MMACHC gene, is a rare genetic disorder that can have significant implications on an individual’s health. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a genetic test specifically designed to identify mutations in the MMACHC gene, providing […]
Methylmalonic Aciduria (MMA) CblB type is a rare genetic disorder that affects the body’s ability to process certain fats and proteins properly, leading to a buildup of methylmalonic acid in the blood. This condition is caused by mutations in the MMAB gene, which plays a crucial role in the metabolism of certain amino acids, fats, […]
Methylmalonic aciduria (MMA) is a rare genetic disorder that affects the body’s ability to metabolize certain fats and proteins, leading to a buildup of methylmalonic acid in the blood. One specific form of this condition, known as the cblA type, is caused by mutations in the MMAA gene. This particular variant of methylmalonic aciduria can […]
Understanding the symptoms of ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency is crucial for early diagnosis and management. This condition, although rare, can have significant impacts on an individual’s health if left undiagnosed or untreated. DNA Labs UAE offers a comprehensive genetic test for this condition, providing a crucial tool for individuals and families seeking answers. […]
Methylcobalamin deficiency, specifically the CblG type, is a rare genetic condition that can have significant health implications. This deficiency is related to the MTR gene, which plays a critical role in the body’s ability to process vitamin B12. Understanding the symptoms of this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers […]
— Understanding the nuances of genetic conditions is crucial for early diagnosis and management. Among these conditions, Methylacetoacetic Aciduria, caused by mutations in the ACAT1 gene, stands out due to its metabolic implications. DNA Labs UAE offers a comprehensive genetic test to identify mutations in the ACAT1 gene, providing vital information for affected individuals and […]
Metachromatic leukodystrophy (MLD) is a rare genetic disorder that affects the body’s ability to produce the enzyme arylsulfatase A (ARSA). Without sufficient levels of this enzyme, sulfatides accumulate in the brain, kidneys, and other tissues, leading to progressive damage. The ARSA gene is responsible for the production of the arylsulfatase A enzyme. Mutations in this […]
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, more commonly known as MELAS syndrome, is a rare genetic disorder that affects multiple systems of the body, particularly the brain and the muscles. This condition is primarily caused by mutations in the mitochondrial DNA, specifically in the MT-TL1 gene. Understanding the symptoms and the importance of […]
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.
