Understanding the complexities of genetic disorders is a challenge that medical science continues to face with determination and innovation. Among these disorders, Spondylo-Megaepiphyseal-Metaphyseal Dysplasia (SMMD), caused by mutations in the NKX3-2 gene, presents a unique set of symptoms and challenges for individuals affected by it. At DNA Labs UAE, we offer a comprehensive genetic test […]
In the realm of genetic testing and diagnosis, advancements have been monumental, enabling us to understand the intricacies of the human genome like never before. Among these advancements, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic tests designed to detect various conditions, including the rare Split-Hand/Foot Malformation Type 6. This […]
Split-hand/foot malformation type 1 (SHFM1), also known as ectrodactyly, is a rare genetic disorder characterized by the malformation of the hands and feet. This condition can vary greatly in severity and can involve the absence of certain fingers or toes, syndactyly (fusion of digits), or the formation of a deep median cleft. When SHFM1 is […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide individuals with valuable insights into their genetic makeup. Among the various tests offered, the MTRR Gene Spina Bifida Folate Sensitive Genetic Test stands out for its importance in assessing the risk of spina bifida, a condition […]
Symptoms of FOXP2 Gene Speech-Language Disorder Type 1 Genetic Test FOXP2 Gene Speech-Language Disorder Type 1 is a condition that affects the neurological development of language and speech capabilities in individuals. This disorder is often identified in early childhood as children start to exhibit significant difficulties in acquiring basic linguistic skills. The FOXP2 gene, a […]
The NFIX Gene Sotos-Like Syndrome is a rare genetic disorder that shares similarities with the traditional Sotos Syndrome, which is characterized by rapid growth during the early years of life, distinctive facial features, and developmental delays. However, the NFIX gene mutation presents its unique set of challenges and symptoms, necessitating specialized genetic testing for accurate […]
Sotos Syndrome Type 1, also known as cerebral gigantism, is a condition that presents a range of physical and cognitive symptoms due to a mutation in the NSD1 gene. DNA Labs UAE offers a comprehensive genetic test for those who suspect they or their loved ones might be affected by this condition. The cost of […]
Understanding Smith-Lemli-Opitz Syndrome Smith-Lemli-Opitz Syndrome (SLOS) is a rare, genetic disorder that affects multiple parts of the body. This condition, which is present from birth, is caused by mutations in the DHCR7 gene. This gene plays a crucial role in the production of cholesterol in the body. Cholesterol, despite its negative reputation, is essential for […]
Understanding the symptoms of COL2A1 Gene SMED Strudwick Type and the significance of genetic testing for this condition is crucial for early diagnosis and management. The COL2A1 gene plays a pivotal role in the development and maintenance of the skeleton and other connective tissues. Mutations in this gene can lead to Spondylometaphyseal Dysplasia (SMED) Strudwick […]
Symptoms of ZBTB16 Gene Skeletal Defects, Genital Hypoplasia, and Mental Retardation Understanding the complex nature of genetic disorders is crucial for early diagnosis and treatment. One such genetic condition involves mutations in the ZBTB16 gene, which can lead to a constellation of symptoms including skeletal defects, genital hypoplasia, and mental retardation. Recognizing these symptoms early […]
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.
