Symptoms of UMOD Gene Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Genetic Test Glomerulocystic kidney disease, characterized by the presence of cysts in the renal cortex and medulla, represents a rare and complex condition. When associated with mutations in the UMOD gene, it can lead to a unique pathology that also encompasses hyperuricemia (elevated uric […]
Nephrology Diseases
Symptoms and Testing information for SLC2A2 Gene Fanconi-Bickel Syndrome Genetic Test
Fanconi-Bickel Syndrome (FBS) is a rare genetic disorder that affects the body’s ability to properly metabolize and utilize carbohydrates, leading to a range of health issues, from poor growth to rickets. At the core of this condition is a mutation in the SLC2A2 gene, which plays a crucial role in glucose transport within the body. […]
Symptoms and Testing information for NNT Gene Glucocorticoid Deficiency Type 4 with or Without Mineralocorticoid Deficiency Genetic Test
Symptoms of NNT Gene Glucocorticoid Deficiency Type 4 with or Without Mineralocorticoid Deficiency Understanding the symptoms of NNT Gene Glucocorticoid Deficiency Type 4, with or without Mineralocorticoid Deficiency, is crucial for early diagnosis and treatment. This rare genetic disorder affects the adrenal glands, leading to insufficient production of certain hormones, primarily cortisol (glucocorticoid) and, in […]
Symptoms and Testing information for MT-TY Gene Focal Segmental Glomerulosclerosis and Dilated Cardiomyopathy MT-TY Related Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) and Dilated Cardiomyopathy are two severe conditions that can have a significant impact on an individual’s health. These diseases can be daunting not just for the patients but also for their families. The MT-TY gene has been identified as a potential contributor to these conditions, highlighting the importance of genetic testing […]
Symptoms and Testing information for NR3C1 Gene Glucocorticoid Resistance Generalized Genetic Test
Genetic testing has become a cornerstone in the diagnosis and management of numerous conditions, offering insights that can significantly influence treatment strategies. Among the various genetic tests available, the NR3C1 Gene Glucocorticoid Resistance Generalized Genetic Test stands out for its crucial role in diagnosing glucocorticoid resistance. This condition, while rare, can have profound implications on […]
Symptoms and Testing information for ACTN4 Gene Focal Segmental Glomerulosclerosis Type 1 Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) is a complex kidney disorder characterized by scarring (sclerosis) in the kidney’s filtering units, known as glomeruli. This condition can lead to severe kidney damage and even kidney failure. One of the genetic forms of this disease, FSGS Type 1, is linked to mutations in the ACTN4 gene. Understanding the symptoms […]
Symptoms and Testing information for TRPC6 Gene Focal Segmental Glomerulosclerosis Type 2 Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) is a disease that attacks the kidney’s filtering units (glomeruli) causing serious scarring which leads to permanent kidney damage and even failure. FSGS can be caused by a variety of factors, including genetic mutations. One such genetic mutation involves the TRPC6 gene, which has been linked to a form of the […]
Symptoms and Testing information for CD2AP Gene Focal Segmental Glomerulosclerosis Type 3 Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) is a disease that attacks the kidney’s filtering units (glomeruli), causing serious scarring which leads to permanent kidney damage and even failure. Among the genetic factors contributing to the development of FSGS, mutations in the CD2AP gene have been identified as a cause for concern. DNA Labs UAE offers a comprehensive […]
Symptoms and Testing information for APOL1 Gene Focal Segmental Glomerulosclerosis Type 4 Susceptibility To Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) is a complex disease that affects the kidney’s filtering units, known as glomeruli, leading to severe scarring. This condition can result in significant kidney damage and, ultimately, kidney failure. Among the various genetic factors associated with FSGS, mutations in the APOL1 gene have been identified as a key contributor, especially in […]
Symptoms and Testing information for INF2 Gene Focal Segmental Glomerulosclerosis Type 5 Genetic Test
Focal Segmental Glomerulosclerosis (FSGS) is a complex kidney disorder characterized by scarring (sclerosis) in the kidney’s filtering units, known as glomeruli. This condition can lead to severe kidney damage and, ultimately, kidney failure. Among the genetic variants contributing to the development of FSGS, mutations in the INF2 gene are significant, leading to a specific subtype […]