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 […]
Senior-Loken syndrome is a rare genetic disorder that affects the kidneys and eyes, leading to progressive loss of kidney function and a form of retinal degeneration known as Leber congenital amaurosis. One of the genes associated with this condition is CEP290, which, when mutated, can lead to Senior-Loken syndrome type 6. Understanding the symptoms of […]
Pseudohypoparathyroidism type 1A (PHP1A) is a rare genetic disorder that affects the body’s ability to regulate certain minerals and hormones, leading to a variety of symptoms. This condition is caused by mutations in the GNAS gene, which plays a critical role in the signaling pathways of several hormones, including those regulating calcium and phosphate. Understanding […]
Senior-Loken syndrome is a rare genetic disorder that affects the kidneys and eyes, leading to a combination of nephronophthisis, which is a form of kidney disease that progresses to end-stage kidney disease, and retinitis pigmentosa, a disorder that causes retinal degeneration and vision loss. The SDCCAG8 gene has been identified as one of the genetic […]
Pseudohypoparathyroidism type 1B (PHP1B) is a rare genetic disorder that affects the body’s ability to regulate calcium and phosphate levels, leading to various physical and developmental symptoms. DNA Labs UAE offers a comprehensive genetic test for the GNAS gene, which is associated with PHP1B, to help diagnose this condition accurately. The cost of the test […]
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.
