Understanding the intricate world of genetics has paved the way for significant advancements in the diagnosis and management of various hereditary conditions. Among these, Weill-Marchesani Syndrome (WMS) stands out due to its rarity and the complex spectrum of symptoms it presents. Specifically, Type 3 WMS, linked to mutations in the LTBP2 gene, poses unique challenges […]
Weill-Marchesani Syndrome (WMS) is a rare genetic disorder that affects the body’s connective tissue, leading to short stature, lens dislocation in the eye, and unique facial features among other symptoms. The syndrome has two main types, with Type 2 being associated with mutations in the FBN1 gene. Understanding the symptoms of FBN1 Gene Weill-Marchesani Syndrome […]
Werner syndrome, also known as adult progeria, is a rare, autosomal recessive disorder characterized by the appearance of premature aging. This condition is caused by mutations in the WRN gene, which plays a crucial role in DNA repair, replication, and recombination. The WRN gene Werner Syndrome Genetic Test is essential for individuals showing symptoms of […]
Wiedemann-Steiner Syndrome (WSS) is a rare genetic disorder characterized by a variety of physical, developmental, and intellectual challenges. This condition is caused by mutations in the KMT2A gene, which plays a significant role in the regulation of gene expression. Understanding the symptoms of WSS and the significance of genetic testing for this condition is crucial […]
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 […]
Witkop Syndrome, also known as Tooth-Nail Syndrome, is a rare genetic condition that affects the development of teeth and nails. This syndrome is primarily associated with mutations in the MSX1 gene. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis and management of the condition. DNA Labs UAE offers a comprehensive […]
— Understanding the symptoms of ERCC4 Gene XFE Progeroid Syndrome is crucial for early detection and management of this rare genetic condition. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including tests for the ERCC4 Gene XFE Progeroid Syndrome. This genetic test is priced at 4400 AED and is a […]
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide valuable insights into various genetic disorders. Among the numerous tests available, the ZIC5 Gene ZIC5 Related Brain Disorders Genetic Test stands out due to its significance in diagnosing brain disorders linked to the ZIC5 […]
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 […]
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 […]
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.
