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 […]
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 […]
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 […]
Symptoms of SCNN1A Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive Genetic Test Pseudohypoaldosteronism type 1 (PHA1) is a rare genetic disorder affecting electrolyte balance and blood pressure regulation. It is caused by mutations in the SCNN1A gene among others, leading to an autosomal recessive inheritance pattern. This condition is characterized by the body’s inability to properly […]
Pseudohypoaldosteronism Type 1 (PHA1) is a rare genetic disorder that affects the body’s ability to properly handle sodium and potassium. This condition can lead to a variety of symptoms and complications, significantly impacting an individual’s quality of life. One of the genes associated with this condition is the NR3C2 gene. Mutations in the NR3C2 gene […]
Understanding the complexities of our genetic makeup is crucial in diagnosing and managing various health conditions. Among these, the CLCN5 gene plays a significant role, particularly in kidney function. Mutations in this gene can lead to a condition characterized by low molecular weight proteinuria with hypercalciuric nephrocalcinosis. DNA Labs UAE is at the forefront of […]
Primary aldosteronism, also known as Conn’s syndrome, is a condition characterized by the overproduction of aldosterone, a hormone responsible for regulating sodium and potassium levels in the blood. This condition can lead to a variety of health issues, including high blood pressure, muscle weakness, and severe electrolyte imbalances. Recent advancements in genetics have identified mutations […]
Symptoms of FMR1 Gene Premature Ovarian Failure Type 1 Genetic Test Premature Ovarian Failure (POF), also known as Primary Ovarian Insufficiency (POI), is a significant health concern affecting women’s reproductive health globally. It is characterized by the loss of normal ovarian function before the age of 40. Among the various factors contributing to this condition, […]
Symptoms of LHCGR Gene Precocious Puberty in Males Precocious puberty refers to the unusually early onset of puberty. Typically, puberty begins between the ages of 8 and 13 in girls and between 9 and 14 in boys. However, in cases of precocious puberty, these developmental changes start much earlier, sometimes as young as 7 in […]
Polycystic Ovary Syndrome (PCOS) is a common condition that affects how a woman’s ovaries work. It has various manifestations, ranging from irregular menstrual cycles to difficulties in conceiving, and is often accompanied by an array of metabolic issues. Among the genetic factors contributing to PCOS, the SULT2B1 gene has garnered attention for its significant role. […]
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.
