Alport Syndrome is a genetic disorder that primarily affects the kidney, leading to progressive loss of kidney function, and can also impact the eyes and the inner ear. The condition is caused by mutations in the genes that produce type IV collagen, a crucial component for the normal functioning of the glomeruli in the kidneys. […]
Alport Syndrome is a genetic disorder that primarily affects the kidneys, leading to chronic kidney disease and, eventually, kidney failure. It also can impact the eyes and the inner ear, potentially leading to vision and hearing loss. The condition is caused by mutations in genes that are essential for the production of a specific type […]
Alport Syndrome is a genetic condition characterized by kidney disease, hearing loss, and eye abnormalities. It primarily affects the basement membranes of the kidneys, ears, and eyes, leading to progressive loss of kidney function and other related symptoms. This condition can be inherited in an autosomal recessive manner, which means that an individual must inherit […]
Adrenocorticotropic Hormone (ACTH) deficiency is a rare condition that can have significant impacts on an individual’s health. The TBX19 gene plays a crucial role in the development and function of the pituitary gland, which in turn influences the production of ACTH. This hormone is essential for regulating the adrenal glands and maintaining the body’s cortisol […]
Adrenal insufficiency congenital, coupled with 46XY sex reversal, partial or complete, is a rare and complex genetic condition that can significantly impact an individual’s health and development. This condition is primarily caused by mutations in the CYP11A1 gene, which plays a crucial role in the production of steroid hormones in the body. These hormones are […]
Acromegaly is a rare hormonal disorder that results from an excess of growth hormone (GH) in the body, often caused by a benign tumor on the pituitary gland. This condition can lead to abnormal growth and size of the hands, feet, and facial features. In some cases, the cause of acromegaly is linked to genetic […]
Understanding the complexities of genetic disorders is essential for early diagnosis and treatment. One such condition, HSD17B10 gene 17-beta hydroxysteroid dehydrogenase X deficiency, is a rare but significant metabolic disorder that affects various bodily functions. DNA Labs UAE offers comprehensive genetic testing to identify this condition, providing crucial insights into potential health risks and management […]
The vascular system plays a critical role in maintaining the homeostasis of the human body, distributing essential nutrients and oxygen to various organs while removing waste products. Genetic abnormalities can significantly impair this system’s functionality, leading to severe health implications. One such genetic concern is related to the GNA13 gene, which, when deficient, can lead […]
In the realm of genetic diagnostics and personalized medicine, understanding the intricate relationships between genes and health conditions is paramount. One such gene, CALCRL, plays a crucial role in the vascular system, and deficiencies in this gene can lead to a range of symptoms and health issues. DNA Labs UAE is at the forefront of […]
In the realm of genetic testing and diagnostics, advancements continue to illuminate our understanding of complex genetic conditions. One such area of focus is the MED13L syndrome, a disorder that stems from variations in the MED13L gene. This condition is associated with a range of developmental and cardiac anomalies, including Transposition of the Great Arteries […]
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.
