Colon cancer is one of the leading causes of cancer-related deaths worldwide, and a significant percentage of these cases are linked to genetic predispositions. One such genetic condition is associated with mutations in the PMS1 gene, leading to a form of hereditary colon cancer known as PMS1-related nonpolyposis hereditary colon cancer. Understanding the symptoms and […]
Oncology Diseases
Symptoms and Testing information for EGFR Gene Nonsmall Cell Lung Cancer Familial Susceptibility to Genetic Test
Lung cancer remains one of the leading causes of cancer-related deaths worldwide, with non-small cell lung cancer (NSCLC) accounting for approximately 85% of all lung cancer cases. Among the genetic factors contributing to the susceptibility and development of NSCLC, mutations in the Epidermal Growth Factor Receptor (EGFR) gene play a significant role. Understanding the symptoms […]
Symptoms and Testing information for MMR Genes Gene MMR Genes Methylation Analysis Genetic Test
Understanding the critical role of genes in our health is a cornerstone of modern medicine. Among these, the Mismatch Repair (MMR) genes hold a pivotal position, especially in the context of cancer predisposition. The MMR system is essential for the cellular repair process, correcting errors that occur during DNA replication. Abnormalities in these genes can […]
Symptoms and Testing information for NPM1 Gene NPM1 Selective Sequencing of Exon 11 Genetic Test
Understanding the genetic basis of diseases has been a cornerstone in modern medical science. Among the various genes scrutinized for their role in human health, the Nucleophosmin 1 (NPM1) gene has garnered significant attention. Mutations in this gene are commonly associated with acute myeloid leukemia (AML), a type of cancer that affects the blood and […]
Symptoms and Testing information for MPL Gene MPL Selective Sequencing of Exon 10 Genetic Test
Understanding the intricacies of our genetic makeup can unlock answers to numerous health-related questions, from predispositions to certain diseases to tailored treatments for individual patients. One such area of focus is the MPL gene, which has garnered attention for its role in various blood disorders. DNA Labs UAE is at the forefront of genetic testing, […]
Symptoms and Testing information for NRAS Gene NRAS Selective Sequencing of Exons 2 and 3 Genetic Test
The NRAS gene is a critical component of the human genome that plays a significant role in cell division, growth, and apoptosis. Mutations in this gene are associated with various types of cancers, including melanoma, leukemia, and colorectal cancer. Understanding the symptoms and undergoing timely genetic testing can be pivotal in the early detection and […]
Symptoms and Testing information for MLH1 Gene Muir-Torre Syndrome Genetic Test
Symptoms of MLH1 Gene Muir-Torre Syndrome Genetic Test Muir-Torre Syndrome (MTS) is a rare, inherited condition that falls under the spectrum of Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC). MTS is characterized by the occurrence of sebaceous gland tumors and at least one visceral malignancy, most commonly colorectal cancer. The genetic underpinning […]
Symptoms and Testing information for PALB2 Gene Pancreatic Cancer Type 3 Susceptibility to Genetic Test
Symptoms of PALB2 Gene Pancreatic Cancer Type 3 Susceptibility to Genetic Test Pancreatic cancer is a formidable disease, often undetected in its early stages due to the lack of specific symptoms. However, advancements in genetic testing have opened new avenues for early detection and personalized treatment strategies. Among these advancements is the genetic test for […]
Symptoms and Testing information for MSH2 Gene Muir-Torre Syndrome Genetic Test
Muir-Torre syndrome (MTS) is a rare genetic condition that is characterized by the occurrence of both skin tumors and internal malignancies. It is considered a subtype of Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC). One of the genes associated with Muir-Torre syndrome is the MSH2 gene. Mutations in this gene can significantly […]
Symptoms and Testing information for CDKN2A Gene Pancreatic Cancer-Melanoma Syndrome Familial Genetic Test
Pancreatic cancer-melanoma syndrome, also known as familial atypical multiple mole melanoma (FAMMM) syndrome, is a condition characterized by an increased risk of developing melanoma and pancreatic cancer. This syndrome is primarily associated with mutations in the CDKN2A gene. Understanding the symptoms and genetic predispositions of this syndrome is crucial for early detection and management. DNA […]