Williams-Beuren Syndrome (WBS) is a rare genetic disorder caused by a deletion of several genes on chromosome 7, specifically at the 7q11.23 locus. This complex condition is characterized by a range of medical and developmental issues, including cardiovascular disease, developmental delays, and distinctive facial features. Understanding the symptoms of Williams-Beuren Syndrome is crucial for early […]
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 […]
Van der Woude Syndrome Type 1 (VWS1) is a genetic condition that is primarily known for its orofacial manifestations. It is an autosomal dominant disorder, meaning that only one copy of the altered gene is sufficient to cause the disorder. The gene implicated in this condition is the IRF6 gene, which plays a crucial role […]
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 […]
Symptoms of GRHL3 Gene Van der Woude Syndrome Type 2 Genetic Test Van der Woude Syndrome Type 2, caused by mutations in the GRHL3 gene, is a rare genetic disorder that affects the development of the face. Recognizing the symptoms early can significantly benefit individuals through timely intervention and management strategies. At DNA Labs UAE, […]
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 […]
Van Maldergem Syndrome Type 2 is a rare genetic disorder that has drawn significant attention within the medical and research communities for its complexity and the implications it holds for affected individuals and their families. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including the FAT4 Gene Van Maldergem Syndrome […]
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 […]
In the realm of genetic testing and diagnostics, the understanding of specific genes and their associated syndromes has become increasingly crucial for early detection and management of various conditions. One such gene that has garnered attention is the HOXD13 gene, known for its association with VACTERL association, a complex genetic condition. DNA Labs UAE stands […]
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 […]
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.
