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 […]
Nephrology Diseases
Symptoms and Testing information for CR2 Gene Immunodeficiency Common Variable Type 7 Genetic Test
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 […]
Symptoms and Testing information for MAGT1 Gene Immunodeficiency X-Linked with Magnesium Defect Epstein-Barr Virus Infection and Neoplasia Genetic Test
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 […]
Symptoms and Testing information for PTH Gene Hypoparathyroidism Genetic Test
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 […]
Symptoms and Testing information for NBAS Gene Infantile Liver Failure Syndrome Type 2 Genetic Test
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 […]
Symptoms and Testing information for GCM2 Gene Hypoparathyroidism Familial Isolated Genetic Test
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 […]
Symptoms and Testing information for FAN1 Gene Interstitial Nephritis Karyomegalic Genetic Test
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). […]
Symptoms and Testing information for GATA3 Gene Hypoparathyroidism Sensorineural Deafness and Renal Dysplasia Genetic Test
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 […]
Symptoms and Testing information for NR1H4 Gene Intrahepatic Cholestasis of Pregnancy NR1H4 Related Genetic Test
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 […]
Symptoms and Testing information for TBCE Gene Hypoparathyroidism-Retardation-Dysmorphism Syndrome Genetic Test
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 […]