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 […]
Symptoms of COL2A1 Gene Spondyloperipheral Dysplasia Genetic Test Spondyloperipheral dysplasia is a form of skeletal disorder characterized by short stature, spinal abnormalities, and peripheral dysostosis. It is caused by mutations in the COL2A1 gene, which plays a crucial role in the development and maintenance of the skeletal system. Recognizing the symptoms early on can be […]
Stiff Skin Syndrome (SSS) is a rare genetic disorder that is often misunderstood due to its rarity and the subtlety of its symptoms in the early stages. This condition is primarily caused by mutations in the FBN1 gene, which plays a crucial role in the development and function of connective tissue in the body. The […]
Stuve-Wiedemann Syndrome (SWS), also known as Schwartz-Jampel Syndrome Type 2, is a rare genetic disorder that is present from birth. This condition is characterized by skeletal abnormalities, muscle weakness, and difficulties in regulating body temperature. It is caused by mutations in the LIFR gene, which plays a crucial role in the development and function of […]
Symptoms of HOXD13 Gene Syndactyly Type 1 Genetic Test Syndactyly Type 1, a condition primarily affecting the fingers and toes, results from mutations in the HOXD13 gene. This genetic disorder is characterized by the fusion of two or more digits, which can lead to difficulties in movement and function, as well as cosmetic concerns. Recognizing […]
Syndactyly is a condition where two or more fingers or toes are fused together. It can vary in severity, from simple webbing of the skin to more complex fusion involving bones, nerves, and other structures. One particular form of this condition, Syndactyly Type 5, has been linked to mutations in the HOXD13 gene. Understanding this […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services that cater to a wide range of genetic conditions, including rare genetic disorders. One such condition is syndactyly associated with the BHLHA9 gene, specifically mesoaxial synostotic syndactyly with phalangeal reduction. This rare genetic disorder affects the development of the hands and feet, […]
Understanding the complexities of genetic disorders, especially those affecting the brain, is crucial for early diagnosis and management. Among the myriad of genes that have been studied for their role in neurological conditions, the TANC2 gene has emerged as a significant player. Mutations in the TANC2 gene are associated with a range of brain disorders, […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into your genetic makeup. Among these, the RBM10 Gene TARP Syndrome Genetic Test is a critical tool for diagnosing TARP Syndrome, a rare genetic condition. This test is not only pivotal for early diagnosis but […]
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.
