Warburg Micro Syndrome (WMS) is a rare genetic disorder characterized by a wide range of physical and developmental abnormalities. One of the genes associated with this condition is RAB3GAP1, and mutations in this gene lead to Warburg Micro Syndrome Type 1. At DNA Labs UAE, we offer a comprehensive genetic test for individuals suspected of […]
Visceral myopathy is a rare genetic disorder that affects the smooth muscles of the gastrointestinal tract, leading to a wide range of digestive problems. One of the genes associated with this condition is the ACTG2 gene. Mutations in this gene can lead to various symptoms that can significantly impact an individual’s quality of life. Understanding […]
Vici syndrome is a rare genetic disorder characterized by a spectrum of clinical manifestations, primarily affecting the brain, immune system, heart, skin, and eyes. It is caused by mutations in the EPG5 gene, which plays a crucial role in the autophagic process, essential for the degradation and recycling of cellular components. Recognizing the symptoms early […]
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 […]
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 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, […]
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 […]
Van den Ende-Gupta syndrome (VDEGS) is a rare genetic disorder characterized by a range of physical anomalies and developmental delays. It is caused by mutations in the SCARF2 gene. This condition, although rare, requires precise diagnosis for appropriate management and intervention. In the UAE, DNA Labs UAE offers a comprehensive genetic test for the SCARF2 […]
Urofacial Syndrome (UFS) or Ochoa Syndrome is a rare genetic disorder characterized by a distinctive facial expression and abnormalities in urinary tract function. The condition, primarily caused by mutations in the HPSE2 gene, leads to what is known as Urofacial Syndrome Type 1. Recognizing the symptoms early and opting for genetic testing can be crucial […]
Urofacial Syndrome, also known as Ochoa Syndrome, is a rare genetic disorder that affects the urinary tract and facial expressions. This condition is often underdiagnosed or misdiagnosed due to the variability of its symptoms. The LRIG2 gene has been identified as a significant factor in the development of Urofacial Syndrome. Understanding the symptoms of 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.
