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 […]
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 […]
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 […]
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 […]
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.
