Renal tubular acidosis (RTA) is a medical condition characterized by the failure of the kidneys to properly acidify the urine. Among the various types of RTA, distal renal tubular acidosis (dRTA) is a significant form that is often inherited in an autosomal recessive manner. The ATP6V0A4 gene has been identified as one of the genetic […]
In the quest to understand and diagnose genetic disorders with precision, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic testing services. Among these, the SLC4A4 gene renal tubular acidosis proximal with ocular abnormalities genetic test is pivotal for diagnosing a rare but significant disorder. This test, priced at 4400 AED, […]
Renal tubular acidosis (RTA) is a medical condition that occurs when the kidneys fail to properly acidify the urine. This failure leads to the blood remaining too acidic, which can cause a host of complications throughout the body. One specific type of RTA, known as type 2 RTA or proximal RTA, can be related to […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide insights into various genetic conditions. One such test is the ACE Gene Renal Tubular Dysgenesis Genetic Test. This detailed examination is specifically designed to detect mutations in the ACE gene, which can lead to […]
Renal Tubular Dysgenesis (RTD) is a rare, autosomal recessive disorder that primarily affects the kidneys. It is characterized by a lack of development (dysgenesis) of the kidney’s proximal tubules, leading to oligohydramnios (low amniotic fluid), which can result in fetal growth restriction and a spectrum of severe clinical manifestations post-birth. The AGT gene plays a […]
Pseudohypoaldosteronism type 1 (PHA1) is a rare genetic condition that affects the body’s ability to properly regulate salt balance. This disorder is characterized by the body’s resistance to the action of aldosterone, a hormone that helps regulate sodium, potassium, and water balance. The SCNN1B gene plays a crucial role in this condition, particularly in its […]
In the realm of genetic diagnostics, understanding the nuances of specific genes and their implications on health is pivotal. One such critical gene is the AGTR1 gene, which, when mutated, can lead to a rare but severe condition known as Renal Tubular Dysgenesis (RTD). DNA Labs UAE stands at the forefront of genetic testing, offering […]
Pseudohypoaldosteronism type 1 (PHA1) is a rare genetic disorder that affects electrolyte balance and blood pressure regulation. It is characterized by the body’s inability to respond properly to aldosterone, a hormone that helps regulate sodium, potassium, and water levels in the body. This condition can lead to various symptoms and complications if not diagnosed and […]
DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services designed to provide individuals with crucial information about their genetic health. Among these essential services is the REN Gene Renal Tubular Dysgenesis Genetic Test, a comprehensive screening designed to identify mutations in the REN gene that can lead to […]
Symptoms of WNK4 Gene Pseudohypoaldosteronism Type 2B Pseudohypoaldosteronism type 2B (PHA2B), also known as Gordon’s syndrome, is a rare genetic disorder that affects the body’s ability to properly regulate blood pressure and electrolyte balance. This condition is caused by mutations in the WNK4 gene, which plays a crucial role in kidney function and the regulation […]
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.
