Polycystic Kidney Disease Type 1 (PKD1) is a severe genetic disorder that affects the kidneys, leading to the development of numerous cysts in these organs. This condition is caused by mutations in the PKHD1 gene and is inherited in an autosomal recessive manner. The disease can lead to various symptoms and complications, significantly impacting an […]
Polycystic Kidney Disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. The PKD2 gene, specifically, is associated with Type 2 Autosomal Dominant Polycystic Kidney Disease (ADPKD), which is less aggressive but still significantly impacts the kidneys and other organs over time. Recognizing the symptoms of this condition early […]
Polycystic liver disease (PLD) is a rare condition that causes numerous cysts to grow in the liver. These cysts can vary in size and may lead to significant enlargement of the liver over time. Although PLD can occur on its own, it is often found in association with polycystic kidney disease (PKD). One of the […]
Polycystic Ovary Syndrome (PCOS) is a common condition affecting women of reproductive age, characterized by hormonal imbalance and metabolism problems that can lead to irregular menstrual periods, infertility, and other health issues. The SULT2A1 gene has been identified as one of the genetic markers associated with PCOS, particularly Type 1. Understanding the symptoms of SULT2A1 […]
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. […]
Nephrotic Syndrome Type 2, caused by mutations in the NPHS1 gene, is a rare but serious condition that affects the kidneys. It is characterized by significant proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Understanding the symptoms and early detection through genetic testing can make a substantial difference in the management and outcome of the condition. DNA Labs […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide insights into various genetic conditions. Among these, the SPINK1 Gene Pancreatitis Genetic Test is particularly notable for its role in detecting predispositions to pancreatitis linked to mutations in the SPINK1 gene. This test is […]
Symptoms of PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test Nephrotic Syndrome Type 3, caused by mutations in the PLCE1 gene, is a rare and severe form of nephrotic syndrome that usually manifests in early childhood. This condition is characterized by significant proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Understanding the symptoms and undergoing genetic testing can […]
In the realm of medical genetics, the understanding and identification of genetic predispositions to certain diseases have become increasingly crucial. Among these genetic conditions, Chronic Early Onset Pancreatitis (CEOP) stands out due to its severe impact on individuals’ health and quality of life. CEOP is often associated with mutations in the CPA1 gene, a critical […]
At DNA Labs UAE, we specialize in providing comprehensive genetic testing services to help individuals and families understand their genetic health. Among the various tests we offer, the LAMB2 Gene Nephrotic Syndrome Type 5 Genetic Test is a crucial diagnostic tool for individuals suspected of having or carriers of this rare genetic disorder. Understanding the […]
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.
