Treacher Collins Syndrome (TCS) is a rare genetic disorder characterized by craniofacial deformities. It is primarily caused by mutations in certain genes, with POLR1D being one of the implicated genes in what is known as Treacher Collins Syndrome Type 2. This condition affects the development of bones and other tissues of the face, leading to […]
Treacher Collins Syndrome Type 1 (TCS1) is a genetic condition that affects the development of bones and other tissues of the face. The symptoms can vary widely among individuals, from mild to severe. The condition is caused by mutations in the TCOF1 gene. Understanding the symptoms and undergoing genetic testing can be crucial for diagnosis, […]
Understanding the intricacies of genetic conditions is crucial for early diagnosis and management. Among these, the MED13L syndrome, associated with the transposition of the great arteries dextro-looped 1 (dTGA), presents a complex genetic anomaly that requires thorough investigation. DNA Labs UAE offers a comprehensive genetic test specifically designed to detect anomalies in the MED13L gene, […]
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 […]
Symptoms of SALL1 Gene Townes-Brocks Syndrome Genetic Test Townes-Brocks Syndrome (TBS) is a rare genetic disorder that can affect multiple organs, including the ears, thumbs, and anus. It is caused by mutations in the SALL1 gene. Recognizing the symptoms early can lead to timely intervention and management of the condition. DNA Labs UAE offers a […]
Symptoms of PAX9 Gene Tooth Agenesis Selective Type 3 Genetic Test Understanding the genetic underpinnings of dental anomalies can lead to significant advancements in diagnosis and treatment strategies. The PAX9 gene plays a crucial role in the development of teeth, and mutations in this gene can lead to tooth agenesis, specifically Selective Type 3. This […]
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 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.
