Understanding the genetic underpinnings of congenital heart defects is crucial for early diagnosis and management. One such genetic condition is the Transposition of the Great Arteries Dextro-Looped 3 (TGA-D3), which is associated with mutations in the GDF1 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, aiming to provide vital information for […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that cater to a wide range of genetic conditions, including rare genetic disorders. One such condition is syndactyly associated with the BHLHA9 gene, specifically mesoaxial synostotic syndactyly with phalangeal reduction. This rare genetic disorder affects the development of the hands and feet, […]
Understanding the complexities of genetic disorders, especially those affecting the brain, is crucial for early diagnosis and management. Among the myriad of genes that have been studied for their role in neurological conditions, the TANC2 gene has emerged as a significant player. Mutations in the TANC2 gene are associated with a range of brain disorders, […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into your genetic makeup. Among these, the RBM10 Gene TARP Syndrome Genetic Test is a critical tool for diagnosing TARP Syndrome, a rare genetic condition. This test is not only pivotal for early diagnosis but […]
Symptoms of Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test Maternal Uniparental Disomy of Chromosome 14 (matUPD(14)) is a rare genetic condition, often associated with a constellation of physical and developmental symptoms known as Temple Syndrome. This condition arises when a child inherits two copies of chromosome 14 from the mother and none from […]
In the realm of genetic diagnostics, the advancement of technology has paved the way for the identification and understanding of rare genetic conditions that were once shrouded in mystery. Among these conditions is Temple-Baraitser Syndrome (TBS), a rare genetic disorder that has been linked to mutations in the KCNH1 gene. At DNA Labs UAE, we […]
Understanding the genetic underpinnings of various conditions is pivotal in the realm of medical science, and this is particularly true for rare syndromes such as Temtamy preaxial brachydactyly syndrome, which is linked to mutations in the CHSY1 gene. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive analyses to uncover the mysteries […]
Split-hand/foot malformation type 1 (SHFM1), also known as ectrodactyly, is a rare genetic disorder characterized by the malformation of the hands and feet. This condition can vary greatly in severity and can involve the absence of certain fingers or toes, syndactyly (fusion of digits), or the formation of a deep median cleft. When SHFM1 is […]
Understanding Temtamy Syndrome: A Genetic Overview Temtamy syndrome, a rare genetic disorder, has garnered significant attention within the medical community due to its unique set of symptoms and genetic origins. At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the C12orf57 Gene Temtamy Syndrome Genetic Test, to help individuals and families […]
In the realm of genetic testing and diagnosis, advancements have been monumental, enabling us to understand the intricacies of the human genome like never before. Among these advancements, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic tests designed to detect various conditions, including the rare Split-Hand/Foot Malformation Type 6. This […]
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.
