Nephrotic Syndrome Type 7, caused by mutations in the DGKE gene, is a rare genetic disorder that affects the kidneys. This condition can lead to significant health issues, including proteinuria, hypoalbuminemia, and edema. At DNA Labs UAE, we offer a comprehensive genetic test to diagnose this condition, ensuring that individuals and families can access the […]
Nephrotic Syndrome Type 8, caused by mutations in the ARHGDIA gene, is a rare genetic disorder that impacts the kidneys’ ability to function properly. This condition can lead to significant health issues, including proteinuria, hypoalbuminemia, severe edema, and susceptibility to infections. Understanding the symptoms and undergoing genetic testing for early detection is crucial for managing […]
Symptoms of COQ8B Gene Nephrotic Syndrome Type 9 Nephrotic Syndrome Type 9, caused by mutations in the COQ8B gene, is a rare genetic disorder that affects kidney function. This condition can lead to significant health issues, including proteinuria, where high levels of protein are found in the urine, hypoalbuminemia, which is characterized by low levels […]
Symptoms of MC4R Gene Obesity Genetic Test Price 4400 AED In the realm of genetic testing, the MC4R Gene Obesity Genetic Test stands out as a crucial tool for understanding the genetic predisposition to obesity. Offered by DNA Labs UAE, this test delves into the genetic makeup of an individual to identify variations in the […]
Symptoms of LEP Gene Obesity Due to Leptin Deficiency Genetic Test Obesity is a complex disease influenced by multiple factors including genetics, environment, and lifestyle choices. Among the genetic factors, mutations in the LEP gene, which encodes the hormone leptin, play a significant role in the development of obesity due to leptin deficiency. Leptin is […]
Nephronophthisis Type 2, caused by mutations in the INVS gene, is a rare genetic disorder that primarily affects the kidneys. This condition is part of a group of diseases known as ciliopathies, which are characterized by abnormalities in the function or structure of cellular cilia. Cilia are microscopic, hair-like structures on the surface of cells […]
Nephronophthisis Type 3 (NPHP3) is a form of an inherited kidney disorder that primarily affects children and young adults. This condition is characterized by inflammation and scarring (fibrosis) of the kidneys. It is a progressive disorder that can lead to renal failure, necessitating comprehensive diagnostic procedures to manage the condition effectively. DNA Labs UAE offers […]
Menkes Disease, a rare genetic disorder, arises from a mutation in the ATP7A gene. This condition affects copper levels in the body, leading to severe developmental issues, neurological problems, and, in many cases, early childhood mortality. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis and management of the disease. DNA […]
Nephronophthisis Type 4 (NPHP4) is a genetic disorder that affects the kidneys and can lead to chronic kidney disease. The NPHP4 gene plays a critical role in the normal functioning and structure of the kidneys. Mutations in the NPHP4 gene can disrupt kidney function, leading to the development of Nephronophthisis Type 4. DNA Labs UAE […]
— The SAMD9 gene plays a critical role in the normal functioning and regulation of cellular processes. Mutations in this gene can lead to a rare but serious condition known as MIRAGE Syndrome. This condition is characterized by a wide range of symptoms that can significantly impact the health and development of affected individuals. DNA […]
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.
