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 […]
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 […]
Nephrotic syndrome type 1, also known as Finnish type nephrosis, is a severe kidney disorder that typically manifests in early childhood. This condition is primarily caused by mutations in the NPHS1 gene, which plays a critical role in the normal functioning of the kidneys. Understanding the symptoms and undergoing genetic testing for NPHS1 gene mutations […]
Nephronophthisis-Like Nephropathy Type 1 is a rare genetic disorder that primarily affects the kidneys. It is caused by mutations in the XPNPEP3 gene and can lead to a variety of symptoms and complications, including chronic kidney disease. Understanding the symptoms and getting a timely diagnosis through genetic testing can significantly impact the management and outcome […]
Nephronophthisis Type 9, caused by mutations in the NEK8 gene, is a rare genetic disorder that primarily affects the kidneys but can also have implications on other organs. Understanding the symptoms and undergoing timely genetic testing can be crucial in managing this condition. DNA Labs UAE offers a comprehensive genetic test for Nephronophthisis Type 9, […]
Nephronophthisis (NPHP) is a genetically heterogenous group of chronic kidney diseases, marked by the progressive loss of kidney function, which often leads to end-stage renal disease. Among its types, Nephronophthisis type 7, caused by mutations in the GLIS2 gene, stands out due to its specific genetic background and clinical manifestations. Understanding the symptoms and undergoing […]
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 […]
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 […]
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 (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 […]
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.
