At DNA Labs UAE, we are dedicated to providing advanced genetic testing services to help individuals understand their genetic predispositions to various conditions. One such condition is the SLC34A1 Gene Nephrolithiasisosteoporosis Hypophosphatemic Type 1, a rare genetic disorder that can significantly impact an individual’s health. Understanding the symptoms of this condition is crucial for early […]
Understanding the complexities of our genetic makeup can be a key factor in managing and preventing various health conditions. Among these, a particular focus has been placed on the SLC9A3R1 gene, associated with Nephrolithiasisosteoporosis Hypophosphatemic Type 2. This condition, while complex, can significantly impact an individual’s quality of life, making awareness and early detection through […]
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 […]
Nephronophthisis is a genetically heterogeneous disorder that primarily affects the kidneys. It is characterized by the inflammation and scarring of the kidney tissue, leading to a progressive loss of kidney function over time. Among the genes associated with this condition, ANKS6 is one of the critical genes implicated in the development of Nephronophthisis Type 16, […]
Nephronophthisis (NPHP) is a genetically and clinically heterogeneous disorder that represents one of the primary causes of chronic kidney disease in children and young adults. Among the various types, Nephronophthisis Type 19, caused by mutations in the DCDC2 gene, is a rare but significant condition that deserves attention. DNA Labs UAE is at the forefront […]
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 […]
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.
