Symptoms of MSX1 Gene Tooth Agenesis Selective Type 1 Genetic Test Tooth agenesis, the developmental absence of one or more teeth, is one of the most common congenital anomalies in humans. Selective tooth agenesis type 1, linked to mutations in the MSX1 gene, affects both the primary and permanent dentition. Recognizing the symptoms early on […]
The FAM58A gene plays a crucial role in human development, influencing various physical attributes and organ functions. Mutations in this gene can lead to a rare but complex condition that manifests through a combination of symptoms, including toe syndactyly, telecanthus, and anogenital and renal malformations. Understanding these symptoms and the availability of genetic testing can […]
Understanding the nuances and implications of genetic disorders is crucial for early diagnosis and appropriate management. One such rare genetic condition is the Three M Syndrome Type 3, caused by mutations in the CCDC8 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, aiming to provide crucial insights for affected individuals and […]
Symptoms of OBSL1 Gene Three M Syndrome Type 2 Genetic Test Three M Syndrome is a rare genetic disorder that is characterized by growth retardation, skeletal abnormalities, and distinctive facial features. Type 2 of this syndrome, specifically, is caused by mutations in the OBSL1 gene. Understanding the symptoms associated with this condition is crucial for […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide patients and healthcare providers with critical information about genetic conditions. Among these, the CUL7 Gene Three M Syndrome Type 1 Genetic Test is a pivotal tool in diagnosing a rare genetic disorder that affects […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into your genetic makeup and potential health risks. Among the advanced tests provided is the WNT3 Gene Tetra-Amelia Autosomal Recessive Genetic Test. This particular test is vital for individuals with a family history of tetra-amelia […]
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 […]
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 […]
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 […]
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 […]
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.
