Beckwith-Wiedemann Syndrome (BWS) is a genetic disorder that affects many parts of the body and is characterized by overgrowth. It is a condition present from birth and varies greatly in how it affects individuals. One of the genes associated with this syndrome is the H19 gene, and testing for abnormalities in this gene can help […]
Understanding Beckwith-Wiedemann Syndrome (BWS) Beckwith-Wiedemann Syndrome (BWS) is a congenital growth disorder that leads to large body size, large organs (organomegaly), and other symptoms. It is a rare condition, affecting approximately 1 in 10,400 newborns worldwide. BWS is associated with abnormalities in the chromosomal region 11p15, where genetic changes increase the risk of developing this […]
Beckwith-Wiedemann Syndrome (BWS) is a complex genetic disorder that affects many parts of the body. It is characterized by a wide range of symptoms and features, which can vary significantly from one individual to another. The syndrome is primarily known for causing overgrowth and an increased risk of developing childhood cancer. The CDKN1C gene plays […]
Basal Cell Nevus Syndrome, also known as Gorlin Syndrome, is a rare genetic condition that significantly increases the risk of developing various cancerous and noncancerous tumors from an early age. This condition is primarily linked to mutations in the PTCH1 gene, but recent studies have shown that mutations in the PTCH2 gene can also lead […]
Symptoms of SUFU Gene Basal Cell Nevus Syndrome Genetic Test Basal Cell Nevus Syndrome, also known as Gorlin Syndrome, is a rare genetic condition that affects various parts of the body. One of the genes associated with this syndrome is the SUFU gene. Mutations in the SUFU gene can lead to an increased risk of […]
Symptoms of PTCH1 Gene Basal Cell Nevus Syndrome Genetic Test Basal Cell Nevus Syndrome, also known as Gorlin Syndrome, is a rare genetic condition that affects various parts of the body. The most common manifestation of this syndrome is the development of multiple basal cell carcinomas, which are a type of skin cancer. This condition […]
Understanding the DNMT3A Gene and Its Link to Acute Myeloid Leukemia Acute Myeloid Leukemia (AML) is a formidable cancer of the blood and bone marrow, the severity of which is compounded by its rapid progression. Among the genetic factors contributing to the development of AML, mutations in the DNMT3A gene have been identified as a […]
Breast cancer is a significant health concern worldwide, affecting millions of women and, albeit less commonly, men. Early detection and understanding one’s genetic predisposition to breast cancer can significantly impact the management and treatment outcomes of this disease. The BRCA1 and BRCA2 gene tests are critical tools in identifying individuals at higher risk of developing […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide valuable insights into various genetic disorders. Among the numerous tests available, the ZIC5 Gene ZIC5 Related Brain Disorders Genetic Test stands out due to its significance in diagnosing brain disorders linked to the ZIC5 […]
— Understanding the symptoms of ERCC4 Gene XFE Progeroid Syndrome is crucial for early detection and management of this rare genetic condition. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including tests for the ERCC4 Gene XFE Progeroid Syndrome. This genetic test is priced at 4400 AED and is a […]
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.
