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). […]
GATA3 gene mutations are associated with a rare but complex condition known as Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) syndrome. This condition, also known as Barakat syndrome, is a genetic disorder that affects several body systems. Understanding the symptoms of this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers a […]
In the realm of medical genetics, understanding the intricate dance of genes and their impact on health is paramount. One such gene, NR1H4, has been linked to Intrahepatic Cholestasis of Pregnancy (ICP), a liver disorder that occurs in some pregnant women. The condition, while temporary, can have significant implications for both mother and child, making […]
Understanding the complexities of genetic disorders is pivotal in the field of medical science. Among these, TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism Syndrome (HRDS) presents a unique set of challenges and symptoms. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including the TBCE Gene HRDS Genetic Test, to help in the diagnosis and […]
Johanson-Blizzard Syndrome (JBS) is a rare genetic disorder that presents a wide range of symptoms affecting multiple organ systems. This condition is primarily caused by mutations in the UBR1 gene, which plays a crucial role in the degradation of proteins and the regulation of pancreatic enzymes. Recognizing the symptoms of JBS is vital for early […]
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.
