— Hypotonia-Cystinuria Syndrome, caused by mutations in the PREPL gene, is a rare genetic condition that affects various body systems. This syndrome is characterized by muscle weakness (hypotonia), reduced muscle mass, growth hormone deficiency, and cystinuria, a condition where high levels of cystine are excreted in the urine, potentially leading to kidney stones. Understanding the […]
At DNA Labs UAE, we understand the importance of genetic testing in diagnosing and managing various health conditions. Among these, the SLC22A12 gene hypouricemia renal type 1 test is crucial for individuals showing symptoms that could indicate this genetic disorder. This comprehensive test, priced at 4400 AED, is designed to identify mutations in the SLC22A12 […]
Hypouricemia Renal Type 2 is a rare condition that affects the kidneys’ ability to process uric acid, leading to abnormally low levels of uric acid in the blood. This condition is genetically inherited and is caused by mutations in the SLC2A9 gene. Understanding the symptoms and undergoing genetic testing can help in the early diagnosis […]
Symptoms of MCM4 Gene Immunodeficiency with Natural Killer Cell Deficiency Genetic Test The MCM4 gene plays a critical role in DNA replication and cellular immunity, particularly in the development and function of natural killer (NK) cells. Mutations in the MCM4 gene can lead to a rare genetic disorder characterized by immunodeficiency and a deficiency in […]
Symptoms of CR2 Gene Immunodeficiency Common Variable Type 7 Common Variable Immunodeficiency (CVID) is a primary immunodeficiency disorder characterized by a low level of antibodies, which can lead to increased susceptibility to infections. Type 7, associated with mutations in the CR2 gene, is one of the rare subtypes of this condition. Understanding the symptoms of […]
Understanding MAGT1 Gene Immunodeficiency The MAGT1 gene plays a crucial role in the human immune system, particularly in its ability to respond to infections and maintain a healthy balance of magnesium within cells. Mutations in the MAGT1 gene can lead to a rare, X-linked condition known as MAGT1 gene immunodeficiency. This condition is characterized by […]
Hypoparathyroidism is a rare condition that occurs when the parathyroid glands in the neck produce insufficient amounts of parathyroid hormone (PTH). This hormone plays a crucial role in regulating calcium, vitamin D, and phosphorus levels in the body. Insufficient levels of PTH lead to low calcium levels and high phosphorus levels in the blood, resulting […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of tests for various genetic conditions. Among these is the NBAS Gene Infantile Liver Failure Syndrome Type 2 Genetic Test, a crucial diagnostic tool for detecting this rare but serious condition in infants. This article aims to provide detailed […]
Understanding the genetic underpinnings of various diseases is crucial in today’s healthcare landscape. Among these, Hypoparathyroidism Familial Isolated, linked to mutations in the GCM2 gene, stands out due to its rarity and the specificity of its symptoms. DNA Labs UAE offers a comprehensive genetic test aimed at diagnosing this condition, helping patients and their families […]
Understanding the Symptoms of FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Disorder Interstitial nephritis is a critical condition that affects the kidneys by causing inflammation of the spaces between the kidney tubules. When this condition is linked to the FAN1 gene, it becomes a part of a rare genetic disorder known as Karyomegalic Interstitial Nephritis (KIN). […]
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.
