At DNA Labs UAE, we are dedicated to providing our clients with comprehensive genetic testing services that help in diagnosing and understanding various genetic disorders. One such condition that has come under increased scrutiny is the syndrome associated with mutations in the CRB2 gene, which can lead to ventriculomegaly and cystic kidney disease. This condition […]
Nephrology Diseases
Symptoms and Testing information for ROBO2 Gene Vesicoureteral reflux type 2 Genetic Test
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to kidney infections and damage. There are various types of VUR, and one of the genetic forms is associated with mutations in the ROBO2 gene, known as Vesicoureteral reflux type 2. Understanding the symptoms […]
Symptoms and Testing information for SOX17 Gene Vesicoureteral reflux type 3 Genetic Test
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to various complications, including urinary tract infections and kidney damage. VUR is categorized into different types, with Type 3 being one of the classifications. Recent studies have identified a genetic link to VUR, specifically […]
Symptoms and Testing information for WDR19 Gene Senior-Loken syndrome type 8 Genetic Test
Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these, the WDR19 gene-related Senior-Loken syndrome type 8 is a condition that demands attention due to its significant impact on individuals’ health. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including tests for this particular syndrome. […]
Symptoms and Testing information for WT1 Gene Wilms tumor type 1 familial Genetic Test
Symptoms of WT1 Gene Wilms Tumor Type 1 Familial Genetic Test Price 4400 AED Wilms tumor, also known as nephroblastoma, is a rare kidney cancer that primarily affects children. It is associated with mutations in the WT1 gene, which plays a crucial role in kidney development. Recognizing the symptoms early can lead to timely diagnosis […]
Symptoms and Testing information for GNAS Gene Pseudohypoparathyroidism type 1C Genetic Test
Pseudohypoparathyroidism type 1C (PHP1C) is a rare genetic disorder that is part of a group of conditions known as pseudohypoparathyroidism. These conditions are characterized by the body’s resistance to parathyroid hormone (PTH), which is crucial for maintaining a balanced calcium and phosphate level in the blood. The GNAS gene, responsible for this condition, plays a […]
Symptoms and Testing information for GNAS Gene Pseudopseudohypoparathyroidism Genetic Test
Pseudopseudohypoparathyroidism is a rare genetic disorder, which involves an abnormality in the GNAS gene. This condition mimics the symptoms of hypoparathyroidism, yet the calcium and phosphorous levels in the blood remain normal. Understanding the symptoms and undergoing genetic testing can be crucial for diagnosis and management. DNA Labs UAE offers a comprehensive GNAS Gene Pseudopseudohypoparathyroidism […]
Symptoms and Testing information for BICC1 Gene Renal cystic dysplasia cystic susceptibility to Genetic Test
Renal cystic dysplasia, a form of kidney malformation, is a condition that can significantly impact an individual’s health and quality of life. Advances in genetic testing have paved the way for early diagnosis and intervention, offering hope to those at risk. DNA Labs UAE is at the forefront of these advancements, providing comprehensive genetic testing […]
Symptoms and Testing information for SLC26A1 Gene Renal dysfunction due to SLC26A1 deficiency Genetic Test
In the realm of genetic diagnostics, the understanding of how specific gene mutations can lead to complex health issues has transformed the approach to treatment and management of various diseases. One such condition that has garnered attention is renal dysfunction caused by SLC26A1 deficiency. This article delves into the symptoms associated with this condition and […]
Symptoms and Testing information for SLC5A2 Gene Renal glucosuria Genetic Test
Renal glucosuria, a condition characterized by the presence of glucose in the urine despite normal blood glucose levels, is primarily caused by mutations in the SLC5A2 gene. This condition is an indication of an abnormal reabsorption of glucose in the kidneys. Understanding the symptoms of SLC5A2 gene renal glucosuria and getting a genetic test can […]