Pancreatitis, an inflammation of the pancreas, can be a debilitating condition that affects many individuals worldwide. It presents in two forms: acute and chronic. While the acute form occurs suddenly and lasts for days, chronic pancreatitis can persist for many years, significantly impacting the quality of life. Among the various causes of pancreatitis, genetic factors […]
Nephrotic Syndrome is a kidney disorder that causes the body to excrete too much protein in the urine. Among its various types, one that stands out due to its genetic nature is caused by mutations in the NPHS2 gene. This condition, often referred to as familial or steroid-resistant nephrotic syndrome, necessitates a deeper understanding and […]
In the realm of genetic testing, advancements have paved the way for identifying and managing various genetic conditions, one of which includes pancreatitis associated with the PRSS1 gene. At DNA Labs UAE, we offer a comprehensive PRSS1 Gene Pancreatitis Genetic Test, designed to detect mutations in the PRSS1 gene that are known to significantly increase […]
Nephrotic Syndrome Type 2, caused by mutations in the NPHS1 gene, is a rare but serious condition that affects the kidneys. It is characterized by significant proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Understanding the symptoms and early detection through genetic testing can make a substantial difference in the management and outcome of the condition. DNA Labs […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide insights into various genetic conditions. Among these, the SPINK1 Gene Pancreatitis Genetic Test is particularly notable for its role in detecting predispositions to pancreatitis linked to mutations in the SPINK1 gene. This test is […]
Nephronophthisis (NPHP) is a genetically and clinically heterogeneous disorder that primarily affects the kidneys. It is the most common genetic cause of chronic kidney disease in children and young adults. NPHP Type 1, caused by mutations in the NPHP1 gene, is a significant subtype of this disorder. Understanding the symptoms and genetic underpinnings of NPHP […]
Nephronophthisis (NPHP) is a genetic disorder that primarily affects the kidneys. It is the most common genetic cause of chronic kidney disease in children and young adults. NPHP Type 12, specifically, is caused by mutations in the TTC21B gene. Understanding the symptoms and getting a timely diagnosis can significantly impact the management and outcome of […]
Nephronophthisis is a genetically heterogeneous group of chronic kidney diseases, characterized by the inflammation and scarring of the kidneys, leading to their eventual failure. Among the genetic variants responsible for this condition, mutations in the WDR19 gene have been identified as a cause of Nephronophthisis Type 13, a rare but serious form of the disease. […]
Nephronophthisis (NPHP) is a genetic disorder that affects the kidneys, leading to their progressive dysfunction. It is the most common genetic cause of end-stage renal disease (ESRD) in children and young adults. Among the various types of NPHP, Type 14, caused by mutations in the ZNF423 gene, is a significant concern due to its autosomal […]
Nephronophthisis (NPHP) is a genetically heterogeneous group of chronic kidney disorders, classified as a form of ciliopathy. The condition primarily affects the kidneys, leading to fibrosis and kidney failure, typically by adolescence or early adulthood. Among the various genes implicated in NPHP, CEP164 plays a crucial role in the development of Nephronophthisis type 15, 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.
