Symptoms of EOGT Gene Adams-Oliver Syndrome Type 4 Genetic Test Adams-Oliver Syndrome (AOS) is a rare genetic condition that can affect multiple parts of the body, including the skin, heart, and limbs. Among its various types, Type 4, caused by mutations in the EOGT gene, presents a unique set of challenges and symptoms for those […]
Amelogenesis Imperfecta (AI) is a congenital disorder that affects the dental enamel, impairing its structure and appearance. Among the various types of AI, Type 1H, linked to mutations in the ITGB6 gene, presents unique challenges and symptoms for those affected. DNA Labs UAE offers a comprehensive genetic test for ITGB6 Gene Amelogenesis Imperfecta Type 1H, […]
Adermatoglyphia, often dubbed as the “immigration delay disease,” is a rare genetic disorder characterized by the absence of fingerprints. This condition not only presents unique challenges in personal identification but also raises intriguing questions about genetic inheritance and variability. At DNA Labs UAE, we offer a comprehensive genetic test for the SMARCAD1 gene, which is […]
Amelogenesis Imperfecta (AI) is a diverse collection of genetic conditions that affect the development of enamel, the hard, outer layer of teeth. Type 2A1, associated with mutations in the KLK4 gene, is one of the subtypes of this condition. DNA Labs UAE offers a comprehensive genetic test for those who may be affected by or […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families gain crucial insights into their genetic makeup, enabling them to make informed health and lifestyle decisions. Among our specialized offerings is the MASP1 Gene 3MC Syndrome Type 1 Genetic Test, a critical tool for diagnosing a rare […]
3MC syndrome is a rare genetic condition that affects various parts of the body. The term “3MC” stands for the three conditions it was initially thought to encompass: Mingarelli, Malpuech, Michels, and Carnevale syndromes. However, it is now understood that these conditions represent a spectrum of a single disorder. 3MC syndrome type 2 is specifically […]
Understanding the genetic makeup of individuals has become a cornerstone in modern medical diagnostics and treatment planning. Among the myriad of genetic conditions that have been identified, achondrogenesis Type 1A, linked to mutations in the TRIP11 gene, stands out due to its rarity and severity. DNA Labs UAE, a leading institution in genetic testing, offers […]
At DNA Labs UAE, we understand the critical importance of accurate genetic testing for families and individuals facing the possibility of genetic conditions. One such rare but severe genetic disorder is Achondrogenesis Type 1B, which is caused by mutations in the SLC26A2 gene. This condition affects the development of bones and cartilage, leading to a […]
Achondrogenesis Type 2, caused by mutations in the COL2A1 gene, is a severe disorder that affects the development of bones and cartilage in the body. This rare genetic condition is part of a group of disorders known as chondrodysplasias, which lead to skeletal abnormalities through the disruption of the normal process of bone growth. Understanding […]
Achondroplasia is a genetic disorder affecting bone growth, leading to dwarfism. This condition is primarily caused by mutations in the FGFR3 gene. Understanding the symptoms of achondroplasia and the significance of genetic testing can provide valuable insights for families and individuals potentially affected by this condition. DNA Labs UAE offers comprehensive genetic testing for achondroplasia […]
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.
