In the realm of personalized medicine and genetic testing, the MDM2 test stands out as a critical tool for assessing cancer risk, particularly in the context of sarcomas and certain other types of cancer. This sophisticated test, offered by DNA Labs UAE, is designed to detect amplifications of the MDM2 gene, which can play a […]
Genetic Diseases
Symptoms and Testing information for MET Amplification NSCLC Test
Non-small cell lung cancer (NSCLC) is one of the most common types of lung cancer, making up about 85% of all lung cancer cases. It’s a disease that can have a significant impact on the lives of those diagnosed with it, as well as their families. Recent advancements in genetic testing have paved the way […]
Symptoms and Testing information for CALR Mutation Analysis Deletion or Insertion in Exon 9 Test
Understanding CALR Mutation Analysis: Deletion or Insertion in Exon 9 The CALR gene, known for its role in coding the calreticulin protein, is essential in maintaining cellular functions, including calcium homeostasis and the proper folding of proteins. Mutations in the CALR gene, particularly deletions or insertions in exon 9, have been identified as significant markers […]
Symptoms and Testing information for CCND1 Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide valuable insights into your health and genetic makeup. One of the critical tests offered by DNA Labs UAE is the CCND1 test, a crucial examination for individuals concerned about their risk of developing certain […]
Symptoms and Testing information for CEBPA Full Gene Mutation Analysis Test
In the realm of genetic testing, the CEBPA Full Gene Mutation Analysis Test stands out as a critical diagnostic tool for individuals at risk of certain types of leukemia. This comprehensive test, offered by DNA Labs UAE for 1800 AED, is pivotal in identifying mutations in the CEBPA gene, which can significantly impact treatment decisions […]
Symptoms and Testing information for Chromosome Breakage Syndrome Test
Chromosome Breakage Syndrome is a group of disorders characterized by the tendency of chromosomes to break more easily than normal. This increased susceptibility to breakage can lead to a variety of clinical manifestations, including developmental delays, intellectual disabilities, congenital anomalies, and an increased risk of cancer. Understanding the symptoms and undergoing timely testing can play […]
Symptoms and Testing information for C-Myc Oncogene Test
DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services aimed at providing accurate and vital information that can significantly impact individuals’ health and treatment options. Among the various tests available, the C-Myc Oncogene Test is one of the critical analyses performed by DNA Labs UAE, designed to detect […]
Symptoms and Testing information for Erythropoietin Receptor Gene Mutation Analysis Test
Erythropoietin (EPO) is a hormone produced by the kidneys that regulates red blood cell production in the bone marrow. Mutations in the Erythropoietin Receptor (EPOR) gene can lead to various hematologic disorders, affecting the body’s ability to produce red blood cells efficiently. Understanding the symptoms of EPOR gene mutations is crucial for timely diagnosis and […]
Symptoms and Testing information for FGFR1 Solid Tumor Test
In the realm of personalized medicine and targeted therapy, understanding the genetic underpinnings of cancer has become crucial. One such advancement is the identification and testing for FGFR1 (Fibroblast Growth Factor Receptor 1) abnormalities in solid tumors. DNA Labs UAE stands at the forefront of this innovation, offering comprehensive FGFR1 Solid Tumor Tests. This test […]
Symptoms and Testing information for Achondroplasia Mutation Analysis FGFR3 Gene G1138A G1138C Test
Achondroplasia is a common form of dwarfism that affects approximately 1 in 25,000 newborns worldwide. It is characterized by a specific set of physical features and health complications, most of which are attributed to mutations in the FGFR3 gene. The G1138A and G1138C mutations within this gene are among the most prevalent causes of this […]