The HOXA13 gene plays a crucial role in the development of the limbs, gastrointestinal tract, and the urinary system. Mutations in this gene can lead to Guttmacher Syndrome, a rare genetic disorder characterized by a spectrum of abnormalities affecting these systems. Recognizing the symptoms of Guttmacher Syndrome is essential for early diagnosis and management. DNA […]
Understanding the intricacies of genetic conditions is crucial for early diagnosis and management. Among these conditions, Duane Retraction Syndrome (DRS) stands out due to its unique manifestations and genetic underpinnings. Specifically, mutations in the SALL4 gene have been linked to this condition, making genetic testing a valuable tool for diagnosis. At DNA Labs UAE, we […]
In the complex world of genetics, understanding the role and impact of specific genes on human health is a crucial aspect of medical science. Among these, the HMG20B gene plays a significant role in various biological processes, including neural development. Dysmorphism in the HMG20B gene can lead to a range of health issues, making it […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and treatment. Among these, TP63 Gene Ectodactyly Ectodermal Dysplasia and Cleft Lip/Palate Syndrome Type 3 (EEC Syndrome Type 3) stands out due to its distinctive symptoms and the critical need for accurate diagnosis. DNA Labs UAE is at the forefront of providing comprehensive genetic […]
Ellis-van Creveld syndrome (EVC) is a rare genetic disorder that affects bone growth, leading to skeletal dysplasia among other symptoms. Understanding the signs and symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for EVC, providing a vital tool for families seeking answers. Symptoms of […]
Ellis-van Creveld syndrome (EvC) is a rare genetic disorder that affects bone growth among other physical manifestations. This condition, inherited in an autosomal recessive manner, primarily involves the shortening of the forearms and lower legs (a condition known as mesomelic dwarfism), polydactyly (extra fingers or toes), and abnormalities in the fingernails and teeth. The EVC2 […]
Understanding the symptoms and genetic underpinnings of complex medical conditions is crucial for effective diagnosis and treatment. One such condition, Epiphyseal Dysplasia Multiple with Myopia and Deafness, is linked to mutations in the COL2A1 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, which is essential for individuals experiencing symptoms or with […]
Faciogenital dysplasia, also known as Aarskog-Scott syndrome, is a rare genetic disorder that primarily affects the development of the face, hands, and genitals. It is caused by mutations in the FGD1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for the […]
Symptoms of ERCC4 Gene Fanconi Anemia Complementation Group Q Genetic Test Fanconi Anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. The ERCC4 gene, also known as FANCQ, has been identified as one of the genes associated with this condition. Individuals with mutations in the ERCC4 gene may develop Fanconi […]
Understanding CANT1 Gene Desbuquois Dysplasia Type 1 Desbuquois Dysplasia is a rare genetic disorder that affects bone development in individuals. It is primarily caused by mutations in the CANT1 gene. This condition is characterized by a variety of symptoms that can significantly impact the quality of life of those affected. Recognizing the symptoms early on […]
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.
